Jones sendromu
Jones sendromu (gingival fibtomatozis-ilerleyici sağırlık sendromu), otosomal dominant yolla aktarılan kalıtsal bir sendromdur. İki temel bileşeni vardır:[1][2][3][4]
- Dişeti büyümeleri,
- İlerleyici sağırlık.
Ayrıca, aşırı kıllanma (hipertrikozis), epilepsi ve zeka geriliği saptanabilir.[1][2][3]
Kaynakça değiştir
- ^ a b Kasaboğlu O, Tümer C, Balcı S. Hereditary gingival fibromatosis and sensorineural hearing loss in a 42-year-old man with Jones syndrome. Journal of Genetic Counseling, 15(2):213-218, 2004
- ^ a b Gita B, Chandrasekaran S, Manoharan P, Dembla G. Idiopathic gingival fibromatosis associated with progressive hearing loss: A nonfamilial variant of Jones syndrome. Contemporary Clinical Dentistry, 5(2):260-263, 2014
- ^ a b Roopa DA, Singh S, Gupta I, Gopal S. Gingival enlargement in a case of variant Jones syndrome: a case report. Journal of Dentistry (Shiraz), 17(1):62-66, 2016
- ^ Coletta RD, Graner E. Hereditary gingival fibromatosis: a systematic review. Journal of Periodontology, 77: 753–764, 2006