Medicine:Jones syndrome
From HandWiki
| Jones syndrome | |
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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.[3] According to Orphanet, it has been reported in two families.[4]
Treatment
Due to the condition's rarity, there are no treatment guidelines.[5]
References
- ↑ "Jones syndrome | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". https://rarediseases.info.nih.gov/diseases/3056/jones-syndrome.
- ↑ "Jones syndrome" (in en-US). https://rarediseases.org/gard-rare-disease/jones-syndrome/.
- ↑ 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), http://accessanesthesiology.mhmedical.com/content.aspx?aid=58071768, retrieved 2021-09-11
- ↑ RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Gingival fibromatosis progressive deafness syndrome" (in en). https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Expert=2027&lng=EN.
- ↑ "Jones syndrome | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". https://rarediseases.info.nih.gov/diseases/3056/jones-syndrome.
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