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X-linked congenital generalized hypertrichosis
rareX-linked congenital generalized hypertrichosis is an extremely rare type of hypertrichosis lanuginosa congenita, a congenital skin disease, which is characterized by hair overgrowth on the entire body in males, and mild and asymmetric hair overgrowth in females. It is associated with a mild facial dysmorphism (anterverted nostrils, moderate prognathism), and, in a kindred, it was also associated with dental anomalies and deafness.
- Identifiers
- MONDO:0010614 OMIM:307150Orphanet:79495
- Also known as
- chromosome Xq27.1 interchromosomal insertion syndrome · congenital generalised hypertrichosis, Macias-Flores type · congenital generalized hypertrichosis, Macias-Flores type · HTC2 · hypertrichosis congenital generalised X-linked
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