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Hereditary gingival fibromatosis

MONDO:0016070

Hereditary gingival fibromatosis (HGF) is a rare benign, slowly progressive, non-inflammatory fibrous hyperplasia of the maxillary and mandibular gingivae that generally occurs with the eruption of the permanent (or more rarely the primary) dentition or even at birth. It presents as a localized or generalized, smooth or nodular overgrowth of the gingival tissues of varying severity. It can be isolated, with autosomal dominant inheritance, or as part of a syndrome.

Also known as: autosomal dominant gingival fibromatosis, autosomal dominant gingival hyperplasia, hereditary gingival fibromatosis, hereditary gingival hyperplasia

53 clinical trials for this condition and its sub-types.

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Sub-types

Fibromatosis, gingival, 2 (2) Fibromatosis, gingival, 1 (0) Fibromatosis, gingival, 3 (0) Fibromatosis, gingival, 4 (0) Fibromatosis, gingival, 5 (0) Fibromatosis, gingival, 6 (0)

Broader categories

Disease (618) Periodontal disorder (241) Musculoskeletal system disorder (196) Hereditary disease (172) Gingival disorder (19) Mouth disorder (17) Gingival overgrowth (16) Human disease (14) Skeletal system disorder (4) Mouth mucosa disorder (3)
Trials to join now! 21 Not yet recruiting 13 Not yet finished but already full! 8 Completed 10 Terminated 1
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