Corpus callosum

Last updated
Corpus callosum
Gray733.png
Corpus callosum from above, front part at the top of the image
Gray720.png
Sagittal section of a brain, front part to the left. The corpus callosum can be seen in the center, in light gray
Details
Pronunciation /ˈkɔːrpəskəˈlsəm/
Part of Human brain
PartsGenu, rostrum, trunk, splenium
FunctionFacilitating communication between the two brain hemispheres, allowing them to share information and coordinate functions like movement, sensory processing, and cognitive tasks
Identifiers
MeSH D003337
NeuroNames 191
NeuroLex ID birnlex_1087
TA98 A14.1.09.241
TA2 5604
FMA 86464
Anatomical terms of neuroanatomy

The corpus callosum (Latin for "tough body"), also callosal commissure, is a wide, thick nerve tract, consisting of a flat bundle of commissural fibers, beneath the cerebral cortex in the brain. The corpus callosum is only found in placental mammals. [1] It spans part of the longitudinal fissure, connecting the left and right cerebral hemispheres, enabling communication between them. It is the largest white matter structure in the human brain, about 10 cm (3.9 in) in length and consisting of 200300 million axonal projections. [2] [3]

Contents

A number of separate nerve tracts, classed as subregions of the corpus callosum, connect different parts of the hemispheres. The main ones are known as the genu, the rostrum, the trunk or body, and the splenium. [4]

Structure

MRI of corpus callosum and its named parts Corpuis callosum.png
MRI of corpus callosum and its named parts
Corpus callosum Corpus callosum.gif
Corpus callosum

The corpus callosum forms the floor of the longitudinal fissure that separates the two cerebral hemispheres. Part of the corpus callosum forms the roof of the lateral ventricles. [5]

The corpus callosum has four main parts – individual nerve tracts that connect different parts of the hemispheres. These are the rostrum, the genu, the trunk or body, and the splenium. [4] Fibres from the trunk and the splenium, known together as the tapetum ("carpet"), form the roof of each lateral ventricle. [6]

The front part of the corpus callosum, towards the frontal lobes, is called the genu ("knee"). The genu curves downward and backward in front of the septum pellucidum, diminishing greatly in thickness. The lower, much thinner part is the rostrum and is connected below with the lamina terminalis, which stretches from the interventricular foramina to the recess at the base of the optic stalk. The rostrum is named for its resemblance to a bird's beak.

The end part of the corpus callosum, towards the cerebellum, is called the splenium. This is the thickest part, and overlaps the tela choroidea of the third ventricle and the midbrain, and ends in a thick, convex, free border. Splenium translates as "bandage" in Greek.

The trunk of the corpus callosum lies between the splenium and the genu.

The callosal sulcus is a sulcus that separates the corpus callosum from the cingulate gyrus.

Relations

On either side of the corpus callosum, the fibers radiate in the white matter and pass to the various parts of the cerebral cortex; those curving forward from the genu into the frontal lobes constitute the forceps minor (also forceps anterior) and those curving backward from the splenium into the occipital lobes, the forceps major (also forceps posterior). [4] Between these two parts is the main body of the fibers, which constitute the tapetum and extend laterally on either side into the temporal lobe, and cover in the central part of the lateral ventricle. The tapetum and anterior commissure share the function of connecting left and right temporal lobes.

The anterior cerebral arteries are in contact with the undersurface of the rostrum; they arch over the front of the genu and are carried along the trunk, supplying the front four-fifths of the corpus callosum. [7]

Neuronal fibers

Fiber tracts from six segments of the corpus callosum.gif

The size, amount of myelination, and density of the fibers in the subregions relate to the functions of the brain regions they connect. [8] Myelination is the process of coating neurons with myelin, which helps the transfer of information between neurons. The process is believed to occur until an individual's thirties with peak growth in the first decade of one's life. [9] Thinner, lightly myelinated fibers are slower conducting and they connect the association and prefrontal areas. Thicker and fast-conducting fibers connect the visual and motor areas. [10]

The tractogram pictured shows the nerve tracts from six segments of the corpus callosum, providing linking of the cortical regions between the cerebral hemispheres. Those of the genu are shown in coral; of the premotor, green; of the sensory-motor, purple; of the parietal, pink; of the temporal, yellow; and of the splenium, blue. [11]

Thinner axons in the genu connect the prefrontal cortex between the two halves of the brain; these fibers arise from a fork-like bundle of fibers from the tapetum, the forceps minor. Thicker axons in the trunk of the corpus callosum interconnect areas of the motor cortex, with proportionately more of the corpus callosum dedicated to supplementary motor regions including Broca's area. The splenium communicates somatosensory information between the two halves of the parietal lobe and the visual cortex at the occipital lobe. These are the fibers of the forceps major. [12] [13]

A study of five- to eighteen-year-olds found a positive correlation between age and callosal thickness. [3]

Variation between sexes

The corpus callosum and its relation to sex has been a subject of debate in the scientific and lay communities for over a century. Initial research in the early 20th century claimed the corpus to be different in size between men and women. That research was, in turn, questioned, and ultimately gave way to more advanced imaging techniques that appeared to refute earlier correlations. However, advanced analytical techniques of computational neuroanatomy developed in the 1990s showed that sex differences were clear, but confined to certain parts of the corpus callosum, and that they correlated with cognitive performance in certain tests. [14] An MRI study found that the midsagittal corpus callosum cross-sectional area is, after controlling for brain size, on average, proportionately larger in females. [15]

Using diffusion tensor sequences on MRI machines, the rate at which molecules diffuse in and out of a specific area of tissue, anisotropy can be measured and used as an indirect measurement of anatomical connection strength. These sequences have found consistent sex differences in human corpus callosal shape and microstructure.[ which? ] [16] [17] [18]

Analysis by shape and size has also been used to study specific three-dimensional mathematical relationships with MRIs, and have found consistent and statistically significant differences between sexes. [19] [20] Specific algorithms have found significant differences between the two sexes in over 70% of cases in one review. [21]

A 2005 study on the sizes and structures of the corpus callosum in transgender people found it to be structurally more in line with their declared gender than their assigned sex. [21]

Correlates of size with handedness

One study reported that the front portion of the human corpus callosum was 0.75 cm2 or 11% larger in left-handed and ambidextrous people than right-handed people. [22] [23] This difference was evident in the anterior and posterior regions of the corpus callosum, but not in the splenium. [22] However, a 2022 meta-analysis failed to confirm any substantial differences in the corpus callosum related to left vs. right- vs. mix-handedness. [24] Others have instead suggested that the degree of handedness negatively correlates with the size of the corpus callosum, meaning that individuals who are capable of using both hands with dexterity would have the largest corpus callosum and vice versa for either left or right hand. [25]

Development

The formation of the corpus callosum begins with the first midline crossing of pioneer axons around week 12 in the prenatal development of the human, [26] or day 15 in the embryogenesis of the mouse. [27]

Clinical significance

Epilepsy

Electroencephalography is used to find the source of electrical activity causing a seizure as part of the surgical evaluation for a corpus callosotomy. EEG cap.jpg
Electroencephalography is used to find the source of electrical activity causing a seizure as part of the surgical evaluation for a corpus callosotomy.

The symptoms of refractory (difficult to treat) epilepsy can be reduced by cutting through the corpus callosum in an operation known as a corpus callosotomy lobotomy paralysis. [28] This is usually reserved for cases in which complex or grand mal seizures are produced by an epileptogenic focus on one side of the brain, causing an interhemispheric electrical storm. The diagnostic work up for this procedure involves an electroencephalogram, MRI, PET scan, and evaluation by a neurologist, neurosurgeon, psychiatrist, and neuroradiologist before a partial lobotomy surgery can be considered. [29]

Failure to develop

Agenesis of the corpus callosum (ACC) is a rare congenital disorder that is one of the most common brain malformations observed in human beings, [30] in which the corpus callosum is partially or completely absent. ACC is usually diagnosed within the first two years of life, and may manifest as a severe syndrome in infancy or childhood, as a milder condition in young adults, or as an asymptomatic incidental finding. Initial symptoms of ACC usually include seizures, which may be followed by feeding problems and delays in holding the head erect, sitting, standing, and walking. Other possible symptoms may include impairments in mental and physical development, hand-eye coordination, and visual and auditory memory. Hydrocephaly may also occur. In mild cases, symptoms such as seizures, repetitive speech, or headaches may not appear for years. Some syndromes often associated with ACC include Aicardi syndrome, Andermann syndrome, Shapiro syndrome, and acrocallosal syndrome.

ACC is usually not fatal. Treatment usually involves management of symptoms, such as hydrocephaly and seizures, if they occur. Although many children with the disorder lead normal lives and have average intelligence, careful neuropsychological testing reveals subtle differences in higher cortical function compared to individuals of the same age and education without ACC. Children with ACC accompanied by developmental delay and/or seizure disorders should be screened for metabolic disorders. [31]

In addition to agenesis of the corpus callosum, similar conditions are hypogenesis (partial formation), dysgenesis (malformation), and hypoplasia (underdevelopment, including too thin).

Other studies have also linked possible correlations between corpus callosum malformation and autism spectrum disorders. [32] [33]

Kim Peek, a savant and the inspiration behind the movie Rain Man , was found with agenesis of the corpus callosum, as part of FG syndrome.

Other conditions

Anterior corpus callosum lesions may result in akinetic mutism or anomic aphasia. See also:

History

The first study of the corpus with relation to gender was by R. B. Bean, a Philadelphia anatomist, who suggested in 1906 that "exceptional size of the corpus callosum may mean exceptional intellectual activity" and that there were measurable differences between men and women. Perhaps reflecting the political climate of the times, he went on to claim differences in the size of the callosum across different races. His research was ultimately refuted by Franklin Mall, the director of his own laboratory. [35]

Of more mainstream impact was a 1982 Science article by Holloway and Utamsing that suggested sex difference in human brain morphology, which related to differences in cognitive ability. [36] Time published an article in 1992 that suggested that, because the corpus is "often wider in the brains of women than in those of men, it may allow for greater cross-talk between the hemispherespossibly the basis for women’s intuition." [37]

Later publications in the psychology literature have raised doubt as to whether the anatomic size of the corpus is actually different. A meta-analysis of 49 studies since 1980 found that, contrary to de Lacoste-Utamsing and Holloway, no sex difference could be found in the size of the corpus callosum, whether or not any account was taken of larger male brain size. [35] A study in 2006 using thin slice MRI showed no difference in thickness of the corpus when accounting for the size of the subject. [38]

Other animals

The corpus callosum is found only in placental mammals, while it is absent in monotremes and marsupials, [39] as well as other vertebrates such as birds, reptiles, amphibians and fish. [40] Other groups do have other brain structures that allow for communication between the two hemispheres, such as the anterior commissure, which serves as the primary mode of interhemispheric communication in marsupials, [41] [42] and which carries all the commissural fibers arising from the neocortex (also known as the neopallium), whereas in placentals, the anterior commissure carries only some of these fibers. [43]

In primates, the speed of nerve transmission depends on the degree of myelination, or lipid coating. This is reflected by the diameter of the nerve axon. In most primates, axonal diameter increases in proportion to brain size to compensate for the increased distance to travel for neural impulse transmission. This allows the brain to coordinate sensory and motor impulses. However, the scaling of overall brain size and increased myelination have not occurred between chimpanzees and humans. This has resulted in the human corpus callosum's requiring double the time for interhemispheric communication as a macaque's. [12] The fibrous bundle at which the corpus callosum appears can and does increase to such an extent in humans that it encroaches upon and wedges apart the hippocampal structures. [44]

Additional images

Related Research Articles

<span class="mw-page-title-main">Holoprosencephaly</span> Failure of the forebrain to develop into two hemispheres during embryonic growth

Holoprosencephaly (HPE) is a cephalic disorder in which the prosencephalon fails to develop into two hemispheres, typically occurring between the 18th and 28th day of gestation. Normally, the forebrain is formed and the face begins to develop in the fifth and sixth weeks of human pregnancy. The condition also occurs in other species.

Alien hand syndrome (AHS) or Dr. Strangelove syndrome is a category of conditions in which a person experiences their limbs acting seemingly on their own, without conscious control over the actions. There are a variety of clinical conditions that fall under this category, most commonly affecting the left hand. There are many similar terms for the various forms of the condition, but they are often used inappropriately. The affected person may sometimes reach for objects and manipulate them without wanting to do so, even to the point of having to use the controllable hand to restrain the alien hand. The occurrence of alien hand syndrome can be usefully conceptualized as a phenomenon reflecting a functional "disentanglement" between thought and action.

<span class="mw-page-title-main">Cerebral hemisphere</span> Left and right cerebral hemispheres of the brain

The vertebrate cerebrum (brain) is formed by two cerebral hemispheres that are separated by a groove, the longitudinal fissure. The brain can thus be described as being divided into left and right cerebral hemispheres. Each of these hemispheres has an outer layer of grey matter, the cerebral cortex, that is supported by an inner layer of white matter. In eutherian (placental) mammals, the hemispheres are linked by the corpus callosum, a very large bundle of nerve fibers. Smaller commissures, including the anterior commissure, the posterior commissure and the fornix, also join the hemispheres and these are also present in other vertebrates. These commissures transfer information between the two hemispheres to coordinate localized functions.

<span class="mw-page-title-main">Cingulate cortex</span> Part of the limbic lobe of the brain cortex

The cingulate cortex is a part of the brain situated in the medial aspect of the cerebral cortex. The cingulate cortex includes the entire cingulate gyrus, which lies immediately above the corpus callosum, and the continuation of this in the cingulate sulcus. The cingulate cortex is usually considered part of the limbic lobe.

<span class="mw-page-title-main">Split-brain</span> Condition of the human brain

Split-brain or callosal syndrome is a type of disconnection syndrome when the corpus callosum connecting the two hemispheres of the brain is severed to some degree. It is an association of symptoms produced by disruption of, or interference with, the connection between the hemispheres of the brain. The surgical operation to produce this condition involves transection of the corpus callosum, and is usually a last resort to treat refractory epilepsy. Initially, partial callosotomies are performed; if this operation does not succeed, a complete callosotomy is performed to mitigate the risk of accidental physical injury by reducing the severity and violence of epileptic seizures. Before using callosotomies, epilepsy is instead treated through pharmaceutical means. After surgery, neuropsychological assessments are often performed.

<span class="mw-page-title-main">Longitudinal fissure</span> Deep groove separating the two cerebral hemispheres of the vertebrate brain

The longitudinal fissure is the deep groove that separates the two cerebral hemispheres of the vertebrate brain. Lying within it is a continuation of the dura mater called the falx cerebri. The inner surfaces of the two hemispheres are convoluted by gyri and sulci just as is the outer surface of the brain.

<span class="mw-page-title-main">Diffuse axonal injury</span> Medical condition

Diffuse axonal injury (DAI) is a brain injury in which scattered lesions occur over a widespread area in white matter tracts as well as grey matter. DAI is one of the most common and devastating types of traumatic brain injury and is a major cause of unconsciousness and persistent vegetative state after severe head trauma. It occurs in about half of all cases of severe head trauma and may be the primary damage that occurs in concussion. The outcome is frequently coma, with over 90% of patients with severe DAI never regaining consciousness. Those who awaken from the coma often remain significantly impaired.

Neuroscience and intelligence refers to the various neurological factors that are partly responsible for the variation of intelligence within species or between different species. A large amount of research in this area has been focused on the neural basis of human intelligence. Historic approaches to studying the neuroscience of intelligence consisted of correlating external head parameters, for example head circumference, to intelligence. Post-mortem measures of brain weight and brain volume have also been used. More recent methodologies focus on examining correlates of intelligence within the living brain using techniques such as magnetic resonance imaging (MRI), functional MRI (fMRI), electroencephalography (EEG), positron emission tomography and other non-invasive measures of brain structure and activity.

<span class="mw-page-title-main">Angular gyrus</span> Gyrus of the parietal lobe of the brain

The angular gyrus is a region of the brain lying mainly in the posteroinferior region of the parietal lobe, occupying the posterior part of the inferior parietal lobule. It represents the Brodmann area 39.

Cerebral atrophy is a common feature of many of the diseases that affect the brain. Atrophy of any tissue means a decrement in the size of the cell, which can be due to progressive loss of cytoplasmic proteins. In brain tissue, atrophy describes a loss of neurons and the connections between them. Brain atrophy can be classified into two main categories: generalized and focal atrophy. Generalized atrophy occurs across the entire brain whereas focal atrophy affects cells in a specific location. If the cerebral hemispheres are affected, conscious thought and voluntary processes may be impaired.

<span class="mw-page-title-main">Anterior cerebral artery</span> Artery supplying the brain

The anterior cerebral artery (ACA) is one of a pair of cerebral arteries that supplies oxygenated blood to most midline portions of the frontal lobes and superior medial parietal lobes of the brain. The two anterior cerebral arteries arise from the internal carotid artery and are part of the circle of Willis. The left and right anterior cerebral arteries are connected by the anterior communicating artery.

<span class="mw-page-title-main">Corpus callosotomy</span> Surgical procedure for epilepsy

A corpus callosotomy is a palliative surgical procedure for the treatment of medically refractory epilepsy. The procedure was first performed in 1940 by William P. van Wagenen. In this procedure, the corpus callosum is cut through, in an effort to limit the spread of epileptic activity between the two halves of the brain. Another method to treat epilepsy is vagus nerve stimulation.

Agenesis of the corpus callosum (ACC) is a rare birth defect in which there is a complete or partial absence of the corpus callosum. It occurs when the development of the corpus callosum, the band of white matter connecting the two hemispheres in the brain, in the embryo is disrupted. The result of this is that the fibers that would otherwise form the corpus callosum are instead longitudinally oriented along the ipsilateral ventricular wall and form structures called Probst bundles.

<span class="mw-page-title-main">Posterior cerebral artery</span> Artery which supplies blood to the occipital lobe of the brain

The posterior cerebral artery (PCA) is one of a pair of cerebral arteries that supply oxygenated blood to the occipital lobe, part of the back of the human brain. The two arteries originate from the distal end of the basilar artery, where it bifurcates into the left and right posterior cerebral arteries. These anastomose with the middle cerebral arteries and internal carotid arteries via the posterior communicating arteries.

<span class="mw-page-title-main">Anterior commissure</span> Bundle of nerve fibers connecting the two temporal lobes of the brain

The anterior commissure is a white matter tract connecting the two temporal lobes of the cerebral hemispheres across the midline, and placed in front of the columns of the fornix. In all but five species of mammal the great majority of fibers connecting the two hemispheres travel through the corpus callosum, which in humans and all non-monotremes is more than 10 times larger than the anterior commissure. Other routes of communication pass through the hippocampal commissure or, indirectly, via subcortical connections. Nevertheless, the anterior commissure is a significant pathway that can be clearly distinguished in the brains of all mammals.

<span class="mw-page-title-main">Commissural fiber</span> Axons that connect the two hemispheres of the brain

The commissural fibers or transverse fibers are axons that connect the two hemispheres of the brain. Huge numbers of commissural fibers make up the commissural tracts in the brain, the largest of which is the corpus callosum.

<span class="mw-page-title-main">Indusium griseum</span>

The indusium griseum, consists of a thin membranous layer of grey matter in contact with the upper surface of the corpus callosum and continuous laterally with the grey matter of the cingulate cortex and inferiorly with the hippocampus. It is vestigial in humans and is a remnant of the former position of the hippocampus in lower animals.

Longitudinal callosal fascicles, or Probst bundles, are aberrant bundles of axons that run in a front-back (antero-posterior) direction rather than a left-right direction between the cerebral hemispheres. They are characteristic of patients with agenesis of the corpus callosum and are due to failure of the callosally-projecting neurons to extend axons across the midline and therefore form the corpus callosum. The inability of these axons to cross the midline results in anomalous axonal guidance and front-to-back projections within each hemisphere, rather than connecting between the hemispheres in the normal corpus callosum.

<span class="mw-page-title-main">Disconnection syndrome</span> Collection of neurological symptoms

Disconnection syndrome is a general term for a collection of neurological symptoms caused – via lesions to associational or commissural nerve fibres – by damage to the white matter axons of communication pathways in the cerebrum, independent of any lesions to the cortex. The behavioral effects of such disconnections are relatively predictable in adults. Disconnection syndromes usually reflect circumstances where regions A and B still have their functional specializations except in domains that depend on the interconnections between the two regions.

<span class="mw-page-title-main">Francisco Aboitiz</span>

Francisco Aboitiz is a Chilean neuroscientist, academic, and author. He is a professor at the Medical School and the Director of the Interdisciplinary Center for Neuroscience NeuroUC at Pontificia Universidad Católica (PUC) de Chile.

References

  1. Velut, S; Destrieux, C; Kakou, M (May 1998). "[Morphologic anatomy of the corpus callosum]". Neuro-Chirurgie. 44 (1 Suppl): 17–30. PMID   9757322.
  2. "Corpus callosum". Queensland Brain Institute. 10 November 2017.
  3. 1 2 Luders, Eileen; Thompson, Paul M.; Toga, Arthur W. (18 August 2010). "The Development of the Corpus Callosum in the Healthy Human Brain". Journal of Neuroscience. 30 (33): 10985–10990. doi:10.1523/JNEUROSCI.5122-09.2010. PMC   3197828 . PMID   20720105.
  4. 1 2 3 Gaillard, Frank. "Corpus callosum | Radiology Reference Article | Radiopaedia.org". radiopaedia.org.
  5. Carpenter, Malcolm (1985). Core text of neuroanatomy (3rd ed.). Baltimore: Williams & Wilkins. pp. 26–32. ISBN   978-0683014556.
  6. Cumming, WJ (March 1970). "An anatomical review of the corpus callosum". Cortex; A Journal Devoted to the Study of the Nervous System and Behavior. 6 (1): 1–18. doi: 10.1016/s0010-9452(70)80033-8 . PMID   4913253.
  7. Ropper, A.; Samuels, M.; Klein, J. (2014). Adams and Victor's Principles of Neurology (10th ed.). McGraw-Hill. p. 798. ISBN   978-0071794794.
  8. Doron, KW; Gazzaniga, MS (September 2008). "Neuroimaging techniques offer new perspectives on callosal transfer and interhemispheric communication". Cortex; A Journal Devoted to the Study of the Nervous System and Behavior. 44 (8): 1023–9. doi:10.1016/j.cortex.2008.03.007. PMID   18672233. S2CID   5641608.
  9. Schlaug, Gotfried; Jäncke, Lutz; Huang, Yanxiong; Staiger, Jochen F; Steinmetz, Helmuth (April 10, 2010). "Increased Corpus Callosum Size in Musicians". Neuropsychologia. 25 (4): 557–577. doi:10.1177/0743558410366594. PMID   8524453. S2CID   145178347.
  10. Aboitiz, F (1992). "Brain connections: interhemispheric fiber systems and anatomical brain asymmetries in humans". Biological Research. 25 (2): 51–61. PMID   1365702.
  11. "NIAAA Publications". pubs.niaaa.nih.gov. Archived from the original on 2021-11-07. Retrieved 2018-09-17.
  12. 1 2 Caminiti, Roberto; Ghaziri, Hassan; Galuske, Ralf; Hof, Patrick R.; Innocenti, Giorgio M. (2009). "Evolution amplified processing with temporally dispersed slow neuronal connectivity in primates". Proceedings of the National Academy of Sciences. 106 (46): 19551–6. Bibcode:2009PNAS..10619551C. doi: 10.1073/pnas.0907655106 . JSTOR   25593230. PMC   2770441 . PMID   19875694.
  13. Hofer, Sabine; Frahm, Jens (2006). "Topography of the human corpus callosum revisited—Comprehensive fiber tractography using diffusion tensor magnetic resonance imaging". NeuroImage. 32 (3): 989–94. doi:10.1016/j.neuroimage.2006.05.044. PMID   16854598. S2CID   1164423.
  14. Davatzikos, C; Resnick, S. M. (1998). "Sex differences in anatomic measures of interhemispheric connectivity: Correlations with cognition in women but not men". Cerebral Cortex. 8 (7): 635–40. doi: 10.1093/cercor/8.7.635 . PMID   9823484.
  15. Ardekani, B. A.; Figarsky, K.; Sidtis, J. J. (2012). "Sexual Dimorphism in the Human Corpus Callosum: An MRI Study Using the OASIS Brain Database". Cerebral Cortex. 23 (10): 2514–20. doi:10.1093/cercor/bhs253. PMC   3767965 . PMID   22891036.
  16. Dubb, Abraham; Gur, Ruben; Avants, Brian; Gee, James (2003). "Characterization of sexual dimorphism in the human corpus callosum". NeuroImage. 20 (1): 512–9. doi:10.1016/S1053-8119(03)00313-6. PMID   14527611. S2CID   31728989.
  17. Westerhausen, René; Kreuder, Frank; Sequeira, Sarah Dos Santos; Walter, Christof; Woerner, Wolfgang; Wittling, Ralf Arne; Schweiger, Elisabeth; Wittling, Werner (2004). "Effects of handedness and gender on macro- and microstructure of the corpus callosum and its subregions: A combined high-resolution and diffusion-tensor MRI study". Cognitive Brain Research. 21 (3): 418–26. doi:10.1016/j.cogbrainres.2004.07.002. PMID   15511657.
  18. Shin, Yong-Wook; Jin Kim, Dae; Hyon Ha, Tae; Park, Hae-Jeong; Moon, Won-Jin; Chul Chung, Eun; Min Lee, Jong; Young Kim, In; Kim, Sun I.; et al. (2005). "Sex differences in the human corpus callosum: Diffusion tensor imaging study". NeuroReport. 16 (8): 795–8. doi:10.1097/00001756-200505310-00003. PMID   15891572. S2CID   11361577.
  19. Kontos, Despina; Megalooikonomou, Vasileios; Gee, James C. (2009). "Morphometric analysis of brain images with reduced number of statistical tests: A study on the gender-related differentiation of the corpus callosum". Artificial Intelligence in Medicine. 47 (1): 75–86. doi:10.1016/j.artmed.2009.05.007. PMC   2732126 . PMID   19559582.
  20. Spasojevic, Goran; Stojanovic, Zlatan; Suscevic, Dusan; Malobabic, Slobodan (2006). "Sexual dimorphism of the human corpus callosum: Digital morphometric study". Vojnosanitetski Pregled. 63 (11): 933–8. doi: 10.2298/VSP0611933S . PMID   17144427.
  21. 1 2 Yokota, Y.; Kawamura, Y.; Kameya, Y. (2005). "Callosal Shapes at the Midsagittal Plane: MRI Differences of Normal Males, Normal Females, and GID". 2005 IEEE Engineering in Medicine and Biology 27th Annual Conference. Vol. 3. pp. 3055–8. doi:10.1109/IEMBS.2005.1617119. ISBN   978-0-7803-8741-6. PMID   17282888. S2CID   351426.
  22. 1 2 Witelson, S. (1985). "The brain connection: The corpus callosum is larger in left-handers". Science. 229 (4714): 665–8. Bibcode:1985Sci...229..665W. doi:10.1126/science.4023705. PMID   4023705.
  23. Driesen, Naomi R.; Raz, Naftali (1995). "The influence of sex, age, and handedness on corpus callosum morphology: A meta-analysis". Psychobiology. 23 (3): 240–7. doi: 10.3758/BF03332028 . S2CID   143304810.
  24. Westerhausen, Rene; Papadatou-Pastou, Marietta (2022). "Handedness and midsagittal corpus callosum morphology: a meta-analytic evaluation". Brain Structure and Function. 227 (2): 545–559. doi: 10.1007/s00429-021-02431-4 . PMC   8843913 . PMID   34851460.
  25. Luders, Eileen; Cherbuin, Nicolas; Thompson, Paul M.; Gutman, Boris; Anstey, Kaarin J.; Sachdev, Perminder; Toga, Arthur W. (2010-08-01). "When more is less: Associations between corpus callosum size and handedness lateralization". NeuroImage. 52 (1): 43–49. doi:10.1016/j.neuroimage.2010.04.016. ISSN   1053-8119. PMC   2903194 . PMID   20394828.
  26. Rakic, P; Yakovlev, PI (January 1968). "Development of the corpus callosum and cavum septi in man". The Journal of Comparative Neurology. 132 (1): 45–72. doi:10.1002/cne.901320103. PMID   5293999. S2CID   40226538.
  27. Rash, BG; Richards, LJ (28 May 2001). "A role for cingulate pioneering axons in the development of the corpus callosum". The Journal of Comparative Neurology. 434 (2): 147–57. doi:10.1002/cne.1170. PMID   11331522. S2CID   29992703.
  28. Clarke, Dave F.; Wheless, James W.; Chacon, Monica M.; Breier, Joshua; Koenig, Mary-Kay; McManis, Mark; Castillo, Edward; Baumgartner, James E. (2007). "Corpus callosotomy: A palliative therapeutic technique may help identify resectable epileptogenic foci". Seizure. 16 (6): 545–53. doi: 10.1016/j.seizure.2007.04.004 . PMID   17521926. S2CID   18192521.
  29. "WebMd Corpus Callotomy". Web MD. July 18, 2010. Archived from the original on July 2, 2010. Retrieved July 18, 2010.
  30. Dobyns, W. B. (1996). "Absence makes the search grow longer". American Journal of Human Genetics. 58 (1): 7–16. PMC   1914936 . PMID   8554070.
  31. "NINDS Agenesis of the Corpus Callosum Information Page: NINDS". RightDiagnosis.com. Archived from the original on 2012-03-24. Retrieved Aug 30, 2011.
  32. Wegiel, Jarek; Kaczmarski, Wojciech; Flory, Michael; Martinez-Cerdeno, Veronica; Wisniewski, Thomas; Nowicki, Krzysztof; Kuchna, Izabela; Wegiel, Jerzy (2018-12-19). "Deficit of corpus callosum axons, reduced axon diameter and decreased area are markers of abnormal development of interhemispheric connections in autistic subjects". Acta Neuropathologica Communications. 6 (1): 143. doi: 10.1186/s40478-018-0645-7 . ISSN   2051-5960. PMC   6299595 . PMID   30567587.
  33. "Autism May Involve A Lack Of Connections And Coordination In Separate Areas Of The Brain, Researchers Find". Medical News Today. Archived from the original on 2011-10-15.
  34. "Cytotoxic lesions of the corpus callosum" . Retrieved 27 October 2024.
  35. 1 2 Bishop, Katherine M.; Wahlsten, Douglas (1997). "Sex Differences in the Human Corpus Callosum: Myth or Reality?" (PDF). Neuroscience & Biobehavioral Reviews. 21 (5): 581–601. doi:10.1016/S0149-7634(96)00049-8. PMID   9353793. S2CID   9909395.
  36. Delacoste-Utamsing, C; Holloway, R. (1982). "Sexual dimorphism in the human corpus callosum". Science. 216 (4553): 1431–2. Bibcode:1982Sci...216.1431D. doi:10.1126/science.7089533. PMID   7089533.
  37. C Gorman (20 January 1992). "Sizing up the sexes". Time. pp. 36–43. As cited by Bishop and Wahlsten.
  38. Luders, Eileen; Narr, Katherine L.; Zaidel, Eran; Thompson, Paul M.; Toga, Arthur W. (2006). "Gender effects on callosal thickness in scaled and unscaled space". NeuroReport. 17 (11): 1103–6. doi:10.1097/01.wnr.0000227987.77304.cc. PMID   16837835. S2CID   14466914.
  39. Keeler, Clyde E. (1933). "Absence of the Corpus callosum as a Mendelizing Character in the House Mouse". Proceedings of the National Academy of Sciences of the United States of America. 19 (6): 609–11. Bibcode:1933PNAS...19..609K. doi: 10.1073/pnas.19.6.609 . JSTOR   86284. PMC   1086100 . PMID   16587795.
  40. Sarnat, Harvey B., and Paolo Curatolo (2007). Malformations of the Nervous System: Handbook of Clinical Neurology, p. 68 [ permanent dead link ]
  41. Ashwell, Ken (2010). The Neurobiology of Australian Marsupials: Brain Evolution in the Other Mammalian Radiation, p. 50
  42. Armati, Patricia J., Chris R. Dickman, and Ian D. Hume (2006). Marsupials, p. 175
  43. Butler, Ann B., and William Hodos (2005). Comparative Vertebrate Neuroanatomy: Evolution and Adaptation, p. 361
  44. Morris, H., & Schaeffer, J. P. (1953). The Nervous system-The Brain or Encephalon. Human anatomy; a complete systematic treatise. (11th ed., pp. 920–921, 964–965). New York: Blakiston.