Zobrazeno 1 - 10
of 492
pro vyhledávání: '"callosal agenesis"'
Publikováno v:
Radiology Case Reports, Vol 19, Iss 12, Pp 6117-6121 (2024)
Corpus callosal agenesis (CCA) is a rare congenital disorder characterized by the partial or complete absence of the corpus callosum, a structure crucial for interhemispheric communication. CCA can occur in isolation or be associated with other anoma
Externí odkaz:
https://doaj.org/article/cd03b6f465674b8195d085b0065fa81c
Publikováno v:
Archives of Medicine and Health Sciences, Vol 12, Iss 1, Pp 120-122 (2024)
West syndrome is a severe form of epilepsy with onset in infancy and early childhood. The characteristic triad described includes infantile spasms (IS), an abnormal electroencephalogram (EEG) pattern referred to as hypsarrhythmia, and developmental r
Externí odkaz:
https://doaj.org/article/4722dddcacf841d1966e39f5d49dfed7
Publikováno v:
Kerala Journal of Ophthalmology, Vol 35, Iss 1, Pp 83-85 (2023)
Aicardi syndrome is a rare neurodevelopmental disorder occurring primarily in female children. It is thought to have X-linked dominant inheritance and the affected male foetuses do not survive to term. A 3-year-old girl child with refractory infantil
Externí odkaz:
https://doaj.org/article/7c4d831a982442e6ac029fbf5cc39a5f
Autor:
Vanessa Siffredi, Younes Farouj, Anjali Tarun, Vicki Anderson, Amanda G. Wood, Alissandra McIlroy, Richard J. Leventer, Megan M. Spencer-Smith, Dimitri Van De Ville
Publikováno v:
NeuroImage, Vol 243, Iss , Pp 118471- (2021)
In the human brain, the corpus callosum is the major white-matter commissural tract enabling the transmission of sensory-motor, and higher level cognitive information between homotopic regions of the two cerebral hemispheres. Despite developmental ab
Externí odkaz:
https://doaj.org/article/4ed11abaccda4c3e9a1b24906bdac15b
Akademický článek
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Akademický článek
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Autor:
Ilan Gobius, Laura Morcom, Rodrigo Suárez, Jens Bunt, Polina Bukshpun, William Reardon, William B. Dobyns, John L.R. Rubenstein, A. James Barkovich, Elliott H. Sherr, Linda J. Richards
Publikováno v:
Cell Reports, Vol 17, Iss 3, Pp 735-747 (2016)
The corpus callosum is the major axon tract that connects and integrates neural activity between the two cerebral hemispheres. Although ∼1:4,000 children are born with developmental absence of the corpus callosum, the primary etiology of this condi
Externí odkaz:
https://doaj.org/article/8818c85899d244be9596722d1db7333e
Colpocephaly is a rare congenital brain malformation resulting in disproportionately large occipital horns of lateral ventricles compared to frontal ones resulting from corpus callosal and other white matter developmental arrest. Colpocephaly can be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::567da3ab687d8219b5f97fa10424ea83
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 11, Iss 6, Pp TD03-TD04 (2017)
Holoprosencephaly (HPE) is a group of structural abnormalities of brain that is an important cause of childhood mortality and morbidity. They usually occur due to impaired midline cleavage of embryonic forebrain i.e., failure of differentiation of t
Externí odkaz:
https://doaj.org/article/8a54fcca874a4021bd54ef4f0f872f8f
Autor:
Taoufik Alsaadi, Tarek M. Shahrour
Publikováno v:
Epilepsy and Behavior Case Reports, Vol 3, Iss C, Pp 1-3 (2015)
The corpus callosum has been proposed as a mechanism of interhemispheric inhibition that allows language dominance to develop [1]. Callosal agenesis or dysgenesis provides a test of this hypothesis, as patients lacking a normal corpus callosum should
Externí odkaz:
https://doaj.org/article/df254817f1084176b52651fac862f11d