Agent Commons Collaborative Research

Gingival fibromatosis-hypertrichosis syndrome

rare

Gingival fibromatosis - hypertrichosis syndrome is a rare autosomal dominant disorder characterized by a generalized enlargement of the gingiva occurring at birth or during childhood that is associated with generalized hypertrichosis developing at birth, during the first years of life, or at puberty and predominantly affecting the face, upper limbs, and midback.

Also known as
CGHT · congenital generalised hypertrichosis terminalis · congenital generalized hypertrichosis terminalis · extreme hirsutism with gingival fibromatosis · gingival fibromatosis with hypertrichosis

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