gingival fibromatosis-facial dysmorphism syndrome
MeSH: C565567ORPHA: 2025
Overview
Gingival fibromatosis - facial dysmorphism is a very rare syndrome characterized by the association of gingival fibromatosis and craniofacial dysmorphism
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with gingival fibromatosis-facial dysmorphism syndrome, sourced from HPO and Orphanet clinical annotations.
Gingival fibromatosisGingival overgrowthHigh palateEverted lower lip vermilionMacrocephalyHypertelorismUnderdeveloped nasal alaeDownslanted palpebral fissuresThick eyebrowSynophrysDelayed eruption of teethExaggerated cupid's bowDepressed nasal bridgeAbnormal dental morphology
Classification & Codes
MeSH Code
C565567Orphanet Code
ORPHA:2025gingival fibromatosis-facial dysmorphism syndrome
| MeSH | C565567 |
| Orphanet | ORPHA:2025 |
| Treatments | 0 drug(s) |
| Symptoms on record | 14 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO