| Literature DB >> 19477093 |
Takashi Shiihara1, Ken-ichi Maruyama, Yoshiyuki Yamada, Akira Nishimura, Naomichi Matsumoto, Mitsuhiro Kato, Satoru Sakazume.
Abstract
Baraitser-Winter syndrome (BaWS) is characterized by iris coloboma, ptosis, hypertelorism, and mental retardation; it is a rare multiple congenital anomaly or a mental-retardation syndrome of unknown etiology. Patients suffering from this syndrome have been also found to show brain anomalies such as pachygyria, subcortical-band heterotopia (SBH), and hippocampal malformations; therefore, these anomalies have been included in the phenotypic spectrum of this syndrome. We report the case of a Japanese boy suffering from BaWS; the patient's brain magnetic resonance imaging scan revealed pachygyria, SBH, and periventricular heterotopia. However, the results of the genome-wide array comparative genomic hybridization did not reveal any chromosomal rearrangements. Copyright (c) 2009 Elsevier B.V. All rights reserved.Entities:
Mesh:
Year: 2009 PMID: 19477093 DOI: 10.1016/j.braindev.2009.04.015
Source DB: PubMed Journal: Brain Dev ISSN: 0387-7604 Impact factor: 1.961