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X-linked recessive inheritance of dysgenesis of corpus callosum in a Chinese family.

作者信息

Kang W M, Huang C C, Lin S J

机构信息

Department of Pediatrics, National Cheng Kung University Hospital, Tainan, Taiwan.

出版信息

Am J Med Genet. 1992 Nov 15;44(5):619-23. doi: 10.1002/ajmg.1320440518.

Abstract

This report describes a new syndrome of dysgenesis of corpus callosum with other anomalies, presenting as microcephaly, mental retardation, spasticity, and unusual facial appearance in 2 Chinese brothers and their maternal cousins. To date, there has not been any case reported in the Chinese population of this syndrome. All 4 patients in this report present with the same unusual face. Hydrocephalus and/or interhemispheric cyst were found among them. This syndrome is transmitted as an X-linked trait. The nosology is reviewed and discussed.

摘要

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