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Х-зчеплений вроджений генералізований гіпертрихоз

ORPHA:79495· ICD-10 Q84.2· X-linked congenital generalized hypertrichosis

Визначення(English summary)

X-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.

Успадкування
X-linked dominant