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Hereditary gingival fibromatosis and sensorineural hearing loss in a 42-year-old man with Jones syndrome.
Genet Couns. 2004; 15(2):213-8.GC

Abstract

Hereditary gingival fibromatosis and sensorineural hearing loss in a 42-year-old man with Jones syndrome: Gingival fibromatosis is a rare disease, which can be seen as an isolated condition or associated with some uncommon syndromes. This case report describes the evaluation and treatment of a 42-year-old male patient with hereditary gingival fibromatosis, sensorineural hearing loss, undescended testis and maxillary odontogenic cyst (Jones Syndrome). Six years follow up of the index patient after the surgery revealed no recurrence of the gingival fibromatosis. This report also describes the anamnestic data of the patient's family that showed progressive deafness and gingival enlargement in three generations.

Authors+Show Affiliations

Hacettepe University, Faculty of Dentistry, Department of Oral and Maxillofacial Surgery, Ankara, Turkey. okasabog@hacettepe.edu.trNo affiliation info availableNo affiliation info available

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

15287422

Citation

Kasaboğlu, O, et al. "Hereditary Gingival Fibromatosis and Sensorineural Hearing Loss in a 42-year-old Man With Jones Syndrome." Genetic Counseling (Geneva, Switzerland), vol. 15, no. 2, 2004, pp. 213-8.
Kasaboğlu O, Tümer C, Balci S. Hereditary gingival fibromatosis and sensorineural hearing loss in a 42-year-old man with Jones syndrome. Genet Couns. 2004;15(2):213-8.
Kasaboğlu, O., Tümer, C., & Balci, S. (2004). Hereditary gingival fibromatosis and sensorineural hearing loss in a 42-year-old man with Jones syndrome. Genetic Counseling (Geneva, Switzerland), 15(2), 213-8.
Kasaboğlu O, Tümer C, Balci S. Hereditary Gingival Fibromatosis and Sensorineural Hearing Loss in a 42-year-old Man With Jones Syndrome. Genet Couns. 2004;15(2):213-8. PubMed PMID: 15287422.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Hereditary gingival fibromatosis and sensorineural hearing loss in a 42-year-old man with Jones syndrome. AU - Kasaboğlu,O, AU - Tümer,C, AU - Balci,S, PY - 2004/8/4/pubmed PY - 2004/10/16/medline PY - 2004/8/4/entrez SP - 213 EP - 8 JF - Genetic counseling (Geneva, Switzerland) JO - Genet Couns VL - 15 IS - 2 N2 - Hereditary gingival fibromatosis and sensorineural hearing loss in a 42-year-old man with Jones syndrome: Gingival fibromatosis is a rare disease, which can be seen as an isolated condition or associated with some uncommon syndromes. This case report describes the evaluation and treatment of a 42-year-old male patient with hereditary gingival fibromatosis, sensorineural hearing loss, undescended testis and maxillary odontogenic cyst (Jones Syndrome). Six years follow up of the index patient after the surgery revealed no recurrence of the gingival fibromatosis. This report also describes the anamnestic data of the patient's family that showed progressive deafness and gingival enlargement in three generations. SN - 1015-8146 UR - https://wwww.unboundmedicine.com/medline/citation/15287422/Hereditary_gingival_fibromatosis_and_sensorineural_hearing_loss_in_a_42_year_old_man_with_Jones_syndrome_ L2 - http://www.diseaseinfosearch.org/result/6504 DB - PRIME DP - Unbound Medicine ER -