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Gingival fibromatosis with sensorineural hearing loss
Familial gingival fibromatosis associated with progressive deafness
Frequency
0.0001%
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.
Epidemiology
Fewer than 100 cases have been published. According to Orphanet, it has been reported in two families.
Treatment
Due to the condition's rarity, there are no treatment guidelines.
↑"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