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Syndrome of microcephaly, microphthalmia, cataracts, and intracranial calcification.

作者信息

Slee J, Lam G, Walpole I

机构信息

Genetic Services of Western Australia, Princess Margaret Hospital for Children, Perth.

出版信息

Am J Med Genet. 1999 Jun 4;84(4):330-3.

Abstract

We present two sisters with microcephaly, developmental delay, marked microphthalmia, congenital cataracts, cerebral and cerebellar hypoplasia, and intracranial calcification. No evidence of intrauterine infection was found. There have been previous reports of microcephaly, intracranial calcification, and an intrauterine infection-like autosomal recessive condition, but the sibs in this report appear to represent a more severe form of such a condition or a previously undescribed entity.

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