Hereditary gingival fibromatosis

Get in touch with RARE Concierge.

Contact RARE Concierge

Hereditary gingival fibromatosis

Synonyms: Autosomal dominant gingival fibromatosis | Autosomal dominant gingival hyperplasia | Hereditary gingival hyperplasia

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.

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.

Reference: Access aggregated data from Orphanet at Orphadata.

Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version April 2024

Newly diagnosed with
Hereditary gingival fibromatosis?

Our RARE Concierge Services Guides are available to assist you by providing information, resources and connections as you navigate your rare disease journey.

Get Concierge Help

Advocacy Organizations

Clinical Trials

For a list of clinical trials in this disease area, please click here.