Jones syndrome
 | You can help expand this article with text translated from the corresponding article in German. (October 2021) Click [show] for important translation instructions.
|
| Jones syndrome | |
|---|---|
| Other names |
|
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
[edit]Fewer than 100 cases have been published.[3] According to Orphanet, it has been reported in two families.[4]
Treatment
[edit]Due to the condition's rarity, there are no treatment guidelines.[5]
References
[edit]- ↑ "Jones syndrome | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". Archived from the original on 2021-09-11. Retrieved 2021-09-11.
- ↑ "Jones syndrome". NORD (National Organization for Rare Disorders). Retrieved 2021-09-11.
- ↑ Bissonnette, Bruno; Luginbuehl, Igor; Marciniak, Bruno; Dalens, Bernard J. (2006), "Jones Syndrome", Syndromes: Rapid Recognition and Perioperative Implications, New York, NY: The McGraw-Hill Companies, retrieved 2021-09-11
- ↑ RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Gingival fibromatosis progressive deafness syndrome". www.orpha.net. Retrieved 2021-09-13.
{{cite web}}: CS1 maint: numeric names: authors list (link) - ↑ "Jones syndrome | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. Archived from the original on 2021-09-11. Retrieved 2021-09-13.
 | This genetic disorder article is a stub. You can help Wikipedia by adding missing information. |