Heterotypic cortex consists of those areas of the mature neocortex that deviate markedly from the homogeneous six-layered internal structure seen in the third trimester of human gestation. A few neocortical areas, such as Brodmann area 17 and the granular insular cortex, undergo modification to more than six layers; and in a few areas, such as Brodmann area 4, the number of layers is reduced. Heterotypic cortex is contrasted to homotypic cortex, which retains the fetal six-layered pattern into adulthood. The number of heterotypic areas is small and the specific areas differ somewhat by species. [1]
A Brodmann area is a region of the cerebral cortex, in the human or other primate brain, defined by its cytoarchitecture, or histological structure and organization of cells.
Brodmann area 10 is the anterior-most portion of the prefrontal cortex in the human brain. BA10 was originally defined broadly in terms of its cytoarchitectonic traits as they were observed in the brains of cadavers, but because modern functional imaging cannot precisely identify these boundaries, the terms anterior prefrontal cortex, rostral prefrontal cortex and frontopolar prefrontal cortex are used to refer to the area in the most anterior part of the frontal cortex that approximately covers BA10—simply to emphasize the fact that BA10 does not include all parts of the prefrontal cortex.
Brodmann area 20, or BA20, is part of the temporal cortex in the human brain. The region encompasses most of the ventral temporal cortex, a region believed to play a part in high-level visual processing and recognition memory.
Brodmann area 21, or BA21, is part of the temporal cortex in the human brain. The region encompasses most of the lateral temporal cortex, a region believed to play a part in auditory processing and language. Language function is left lateralized in most individuals. BA21 is superior to BA20 and inferior to BA40 and BA41.
Brodmann area 4 refers to the primary motor cortex of the human brain. It is located in the posterior portion of the frontal lobe.
The primary somatosensory cortex is located in the postcentral gyrus, and is part of the somatosensory system. It was initially defined from surface stimulation studies of Wilder Penfield, and parallel surface potential studies of Bard, Woolsey, and Marshall. Although initially defined to be roughly the same as Brodmann areas 3, 1 and 2, more recent work by Kaas has suggested that for homogeny with other sensory fields only area 3 should be referred to as "primary somatosensory cortex", as it receives the bulk of the thalamocortical projections from the sensory input fields.
Brodmann area 24 is part of the anterior cingulate in the human brain.
The Brodmann area 32, also known in the human brain as the dorsal anterior cingulate area 32, refers to a subdivision of the cytoarchitecturally defined cingulate cortex. In the human it forms an outer arc around the anterior cingulate gyrus. The cingulate sulcus defines approximately its inner boundary and the superior rostral sulcus (H) its ventral boundary; rostrally it extends almost to the margin of the frontal lobe. Cytoarchitecturally it is bounded internally by the ventral anterior cingulate area 24, externally by medial margins of the agranular frontal area 6, intermediate frontal area 8, granular frontal area 9, frontopolar area 10, and prefrontal area 11-1909. (Brodmann19-09).
Brodmann Area 14 is one of Brodmann's subdivisions of the cerebral cortex in the brain. It was defined by Brodmann in the guenon monkey . While Brodmann, writing in 1909, argued that no equivalent structure existed in humans, later work demonstrated that area 14 has a clear homologue in the human ventromedial prefrontal cortex.
The allocortex is one of two types in the cerebral cortex, the other being the neocortex. It is characterized by having just three or four cell layers, in contrast with the six layers of the neocortex, and takes up a much smaller area than the neocortex. There are three subtypes of allocortex: the paleocortex, the archicortex, and the periallocortex – a transitional zone between the neocortex and the allocortex.
Brodmann area 13 is part of the insula, a subdivision of the cerebral cortex as defined by cytoarchitecture. The insula is covered by frontal, temporal and parietal operculum and therefore sometimes ignored as a Brodmann area.
Brodmann area 16 is a subdivision of the cerebral cortex of the guenon defined on the basis of cytoarchitecture. It is a relatively undifferentiated cortical area that Brodmann regarded as part of the insula because of the relation of its innermost multiform layer (VI) with the claustrum (VICl). The laminar organization of cortex is almost totally lacking. The molecular layer (I) is wide as in area 15 of Brodmann-1905. The space between layer I and layer VI is composed of a mixture of pyramidal cells and spindle cells with no significant number of granule cells. Pyramidal cells clump in the outer part to form glomeruli similar to those seen in some of the primary olfactory areas (Brodmann-1905).
Brodmann area 26 is the name for a small part of the brain.
Brodmann area 28 is a subdivision of the cerebral cortex defined on the basis of cytoarchitecture. It is located on the medial aspect of the temporal lobe and is part of the entorhinal cortex (Brodmann-1909).
Brodmann area 29, also known as granular retrolimbic area 29 or granular retrosplenial cortex, is a cytoarchitecturally defined portion of the retrosplenial region of the cerebral cortex. In the human it is a narrow band located in the isthmus of cingulate gyrus. Cytoarchitecturally it is bounded internally by the ectosplenial area 26 and externally by the agranular retrolimbic area 30 (Brodmann-1909).
Brodmann area 43, the subcentral area, is a structurally distinct area of the cerebral cortex defined on the basis of cytoarchitecture. Along with Brodmann Area 1, 2, and 3, Brodmann area 43 is a subdivision of the postcentral region of the brain, suggesting a somatosensory function. The histological structure of Area 43 was initially described by Korbinian Brodmann, but it was not labeled on his map of cortical areas.
Cytoarchitecture, also known as cytoarchitectonics, is the study of the cellular composition of the central nervous system's tissues under the microscope. Cytoarchitectonics is one of the ways to parse the brain, by obtaining sections of the brain using a microtome and staining them with chemical agents which reveal where different neurons are located.
Agranular cortex is a cytoarchitecturally defined term denoting the type of heterotypic cortex that is distinguished by its relative thickness and lack of granule cells. Examples are Brodmann area 30, the agranular insula, and the precentral gyrus, the site of the primary motor cortex. An area of cortex that is only slightly granulated is termed dysgranular.
The external granular layer of the cerebral cortex is commonly known as layer II. It is different from the internal granular layer of the cerebral cortex.
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