Warburg M
Eye Clinic for Patients with Multiple Handicaps, Gentofte Hospital, Denmark.
Eur J Pediatr. 1987 Sep;146(5):450-2. doi: 10.1007/BF00441592.
Retinal dysplasia and agyria without cortical lamination are the constant findings in this autosomal recessive syndrome. There may also be anterior chamber malformations, cataract, and microphthalmos. Brain autopsies have shown a variety of associated malformations such as posterior encephalocele, Arnold-Chiari malformation, agenesis of the septum pellucidum and of the corpus callosum, agenesis of the vermis and hypoplasia of the cerebellum. Muscular dystrophy is probably present in most of these patients. Within the last few years, over 20 cases with a complete autopsy have been described. The syndrome should be differentiated from other syndromes with retinal non-attachment and retinal dysplasia, and from syndromes with hydrocephalus or encephalocele without these ocular features.
视网膜发育异常和无脑回且无皮质分层是这种常染色体隐性综合征的常见表现。还可能存在前房畸形、白内障和小眼症。脑部尸检显示有多种相关畸形,如后颅窝脑膨出、阿诺德-奇亚里畸形、透明隔和胼胝体发育不全、小脑蚓部发育不全和小脑发育不全。这些患者中的大多数可能患有肌肉萎缩症。在过去几年中,已经描述了20多例进行了完整尸检的病例。该综合征应与其他伴有视网膜脱离和视网膜发育异常的综合征,以及伴有脑积水或脑膨出但无这些眼部特征的综合征相鉴别。