X-linked congenital generalized hypertrichosis

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.

Also known as: Macias Flores-Garcia Cruz-Rivera syndrome, congenital generalised hypertrichosis, Macias-Flores type, congenital generalized hypertrichosis, Macias-Flores type, hypertrichosis, congenital generalized, X-linked dominant, Cgh, HTC2, Macias-Flores Garcia-Cruz Rivera syndrome, chromosome Xq27.1 Interchromosomal insertion syndrome

0 clinical trials for this condition and its sub-types, 0 tagged with X-linked congenital generalized hypertrichosis itself.