Jones syndrome explained
| Jones syndrome |
| Synonym: | - Gingival fibromatosis with progressive deafness
- GFD
- Gingival fibromatosis with sensorineural hearing loss
- Familial gingival fibromatosis associated with progressive deafness[1]
|
Jones syndrome is an extremely rare disorder characterized by gingival fibromatosis and sensorineural hearing loss. The condition is an inherited but the underlying genetic cause is currently unknown.[2]
Epidemiology
Fewer than 100 cases have been published. According to Orphanet, it has been reported in two families.[3]
Treatment
Due to the condition's rarity, there are no treatment guidelines.[4]
Notes and References
- Web site: Jones syndrome | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program.
- Web site: Jones syndrome. 2021-09-11. NORD (National Organization for Rare Disorders). en-US.
- Web site: RESERVED. INSERM US14-- ALL RIGHTS. Orphanet: Gingival fibromatosis progressive deafness syndrome. 2021-09-13. www.orpha.net. en.
- Web site: Jones syndrome Genetic and Rare Diseases Information Center (GARD) – an NCATS Program. 2021-09-13. rarediseases.info.nih.gov.
