PMID: 4017282Jun 1, 1985

Dominantly inherited syndrome of microcephaly and congenital lymphedema

Clinical Genetics
A K Leung


A Chinese family is reported in which microcephaly and congenital lymphedema have been observed in at least 4 generations. This combination of symptoms can be presumed to represent a rare but well defined hereditary syndrome transmitted by an autosomal dominant gene.


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