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A genetic association between microcephaly and lymphedema.

Identifieur interne : 005D68 ( PubMed/Checkpoint ); précédent : 005D67; suivant : 005D69

A genetic association between microcephaly and lymphedema.

Auteurs : C A Crowe ; L H Dickerman

Source :

RBID : pubmed:3706402

Descripteurs français

English descriptors

Abstract

We discuss a family in which microcephaly and lymphedema are co-segregating as an apparently autosomal or X-linked dominant trait. A review of each malformation is presented with reference to the known genetic patterns of each. This combination of microcephaly and lymphedema may be a unique syndrome, previously undescribed because of subtleties of expression in affected individuals.

DOI: 10.1002/ajmg.1320240116
PubMed: 3706402


Affiliations:


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pubmed:3706402

Le document en format XML

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