نتایج جستجو برای: corpus callosum agenesis (cca)

تعداد نتایج: 75383  

Journal: :iranian journal of child neurology 0
muhammad saeed* 1. king faisal specialist hospital & research center, riyadh, saudi arabia anwar ul haq 1. king faisal specialist hospital & research center, riyadh, saudi arabia khaqan qadir 2. military hospital riyadh, riyadh, saudi arabia

how to cite this article: saeed m, haq a, qadir kh.bart’s syndrome associated corpus callosum agenesis and choanal atresia. iran j child neurol. 2014 autumn;8(4): 76-79. abstract objective bart’s syndrome is defined as congenital localized absence of skin, and associated with epidermolysis bullosa. a newborn with bart’s syndrome is reported because it is a very rare condition, especially when a...

Journal: :Neurology 2011
R M Hanna S E Marsh D Swistun L Al-Gazali M S Zaki G M Abdel-Salam A Al-Tawari L Bastaki H Kayserili A Rajab B Boglárka R B Dietrich W B Dobyns C L Truwit S Sattar N A Chuang E H Sherr J G Gleeson

OBJECTIVE We sought to create a classification system for pediatric corpus callosal abnormalities (CCA) based upon midline sagittal brain MRI. We used the term CCA for patients with structural variants of the corpus callosum, excluding patients with interhemispheric cyst variant or pure dysplasia without hypoplasia. Currently, no system exists for nonsyndromic forms of CCA, and attempts to crea...

Alireza Jashni Motlagh Mousa Ahmadpourkacho Yadollah Zahedpasha

Background: X-linked lissencephaly with ambiguous genitalia (XLAG) is a recently described genetic disorder, in which patients present with lissencephaly, agenesis of the corpus callosum, refractory epilepsy of neonatal onset, acquired microcephaly, and male genotype with ambiguous genitalia. XLAG is responsible for a severe neurological disorder of neonatal onset in boys. A gyration defect con...

Journal: :Military Medical and Pharmaceutical Journal of Serbia 2003

2014
Ester Pereira Monica Rebollo Polo Jordi Muchart López Thais Agut Quijano Alfredo García-Alix Carmen Fons

The agenesis of the corpus callosum results from a failure in the development of the largest fiber bundle that connects cerebral hemispheres. Patient's outcome is influenced by etiology and associated central nervous system malformations. We describe a child with Turner syndrome (TS) mosaicism, with particular phenotype features and a complete agenesis of the corpus callosum. To our knowledge, ...

Journal: :iranian journal of child neurology 0
ravish singhal* pg resident, department of pediatrics, government multispecialty hospital, sector-16, chandigarh, india sadbhavna pandit head of the department pediatrics, government multispeciality hospital, sector-16, chandigarh, india ashok saini government multispeciality hospital, sector-16, chandigarh paramjit singh medical officer, pediatrics, government multispecialty hospital, sector-16, chandigarh, india neeraj dhawan medical officer, pediatrics, government multispecialty hospital, sector-16, chandigarh, india

how to cite this article: singhal r, pandit s, saini a, singh p, dhawan n. the acrocallosal syndrome in a neonate with further widening of phenotypic expression. iran j child neurol. 2014 spring;8(2):60-64.   the presentation of the typical characteristics of the acrocallosal syndrome (acls) are hypoplasia/agenesis of corpus callosum, moderate to severe mental retardation, characteristic cranio...

Journal: :AJNR. American journal of neuroradiology 2010
D J Warren D J A Connolly P D Griffiths

BACKGROUND AND PURPOSE There is gathering evidence to suggest that agenesis of the corpus callosum is associated with delayed fetal sulcation; it is possible that the corpus callosum facilitates normal gyral development. In this paper we sought to confirm whether delayed sulcation is found in fetuses with isolated agenesis of the corpus callosum as judged by in utero MR imaging. MATERIALS AND...

Journal: :genetics in the 3rd millennium 0
فائزه مجاهدی faezeh mojahedi

microphthalmia is defined as a globe with a total axial length that is at least two standard deviations below the mean for age. it may be isolated or part of a syndrome with other associated anomalies. causes can be divided into environmental, heritable or unknown. some researchers believe that microphthalmia and anophthalmia belong to one family. unilateral and bilateral anophtalmia have been ...

Journal: :Neurosciences 2001
A Chacko R Koul D K Sankhla

OBJECTIVE The objectives are to analyse corpus callosum agenesis in children with various neurological problems in a hospital set-up, and to study the neurological and systemic abnormalities associated with this condition. METHODS The children with various neurological problems who underwent computerized tomography brain from January 1993 to December 1997, and were found to have corpus callos...

Journal: :Swiss medical weekly 2006
Gp Ramelli N Zanda M Wyttenbach L Bronz A Schnider

The post-natal development of 6 patients with complete agenesis of the corpus callosum was assessed. The diagnosis of agenesis of the corpus callosum had been suspected prenatally in 3 cases. In the remaining 3 cases diagnostic neuro-imaging was performed because of partial seizures (n = 2) and pendular nystagmus (n = 1). The neurological examination was normal in all patients with the exceptio...

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