Dominantly inherited syndrome of microcephaly and congenital lymphedema
- 1 June 1985
- journal article
- research article
- Published by Wiley in Clinical Genetics
- Vol. 27 (6) , 611-612
- https://doi.org/10.1111/j.1399-0004.1985.tb02047.x
Abstract
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.Keywords
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