Ambras type hypertrichosis universalis congenita

Congenital generalized hypertrichosis, Ambras type is an extremely rare type of hypertrichosis lanuginosa congenita, a congenital skin disease, that is characterized by the presence of vellus-type hair on the entire body, especially on the face, ears and shoulders, with the exception of palms, soles, and mucous membranes. Facial and dental anomalies can also be observed, such as triangular, coarse face, bulbous nasal tip, long palpebral fissures, delayed tooth eruption and absence of teeth.

Also known as: Ambras syndrome, HTC1, HTC 1, congenital generalised hypertrichosis, Ambras type, congenital generalized hypertrichosis, Ambras type, hypertrichosis universalis congenita Ambras type, hypertrichosis universalis congenita, Ambras type, hypertrichosis, congenital generalised

0 clinical trials for this condition and its sub-types, 0 tagged with Ambras type hypertrichosis universalis congenita itself.