Brief clinical report: A genetic association between microcephaly and lymphedema

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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.