Congenital generalized hypertrichosis, Ambras type OMIM:145701 MESH:C536605 ICD10:Q84.2 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. orphanet Ambras syndrome Malformation syndrome with skin/mucosae involvement Rare genetic skin disease Eyebrow/eyelashes hypertrichosis