Autosomal recessive bilateral frontal polymicrogyria with ectopia lentis and chorioretinal dystrophy

常染色体隐性遗传性双侧额叶多小脑回畸形伴晶状体异位和脉络膜视网膜营养不良

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Abstract

Polymicrogyria is a type of cortical dysplasia with cortical organizational defect. Bilateral polymicrogyria are distinct with genetic basis in a subset. We hereby report a case of bilateral frontal polymicrogyria (BFP) in association with chorioretinal dystrophy and ectopia lentis (EL) in a 26-year-old lady born of a consanguineous parentage. Her male sibling also had chorioretinal dystrophy and EL. This combination of autosomal recessive inheritance has not been reported earlier in the literature and suggests a role of connective tissue genes in BFP.

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