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Medical Definition of Goltz syndrome
1. A genetic skin disease characterised by hypoplasia of the dermis, herniations of fat, and hand anomalies. It is found exclusively in females and transmitted as an x-linked dominant trait. (12 Dec 1998)
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1. A genetic skin disease characterised by hypoplasia of the dermis, herniations of fat, and hand anomalies. It is found exclusively in females and transmitted as an x-linked dominant trait. (12 Dec 1998)