Gingival fibromatosis-hypertrichosis syndrome

Disease Export to PDF
Name:
Gingival fibromatosis-hypertrichosis syndrome
Description:
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.
ORPHAcode:
2026
Synonyms:
CGHT
Congenital generalized hypertrichosis terminalis
Hirsutism-congenital gingival hyperplasia syndrome
Hypertrichosis with or without gingival hyperplasia
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Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14