Hereditary gingival fibromatosis
MONDO:0016070Hereditary 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
23 clinical trials for this condition and its sub-types, 0 tagged with Hereditary gingival fibromatosis itself.
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Sub-types of Hereditary gingival fibromatosis
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Fibromatosis, gingival, 2 2 trials
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Fibromatosis, gingival, 1 0 trials
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Fibromatosis, gingival, 3 0 trials
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Fibromatosis, gingival, 4 0 trials
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Fibromatosis, gingival, 5 0 trials
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Fibromatosis, gingival, 6 0 trials
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