| Literature DB >> 10340646 |
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.Entities:
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Year: 1999 PMID: 10340646
Source DB: PubMed Journal: Am J Med Genet ISSN: 0148-7299