Straussberg R, Gross S, Amir J, Gadoth N
Child Developmental Center, Hasharon Hospital-Gold Medical Center, Petah-Tiqva, Israel.
Clin Genet. 1996 Dec;50(6):498-501. doi: 10.1111/j.1399-0004.1996.tb02721.x.
Pachygyria is a rare development disorder resulting from impaired neuronal migration. Usually, it is a sporadic phenomenon, but rare dominant or autosomal recessive syndromes are known. This report describes a family in which the parents are first cousins and three of the siblings suffer from moderate mental retardation, pachygyria and strabismus. It is suggested that this is a distinct type of autosomal recessive pachygyria.
巨脑回畸形是一种由神经元迁移受损导致的罕见发育障碍。通常,它是一种散发性现象,但已知有罕见的显性或常染色体隐性综合征。本报告描述了一个家庭,父母是近亲,三个兄弟姐妹患有中度智力迟钝、巨脑回畸形和斜视。提示这是一种独特类型的常染色体隐性巨脑回畸形。