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Familial gingival fibromatosis associated with progressive deafness in five generations of a family.
Birth Defects Orig Artic Ser. 1977; 13(3B):195-201.BD

Abstract

Gingival hyperplasia may be inherited in a variety of ways, usually in an autosomal dominant or autosomal recessive manner. Additional phenotypic abnormalities are frequently associated with the gingival hyperplasia. To our knowledge, the family described here represents the first instance of autosomal dominantly inherited gingival hyperplasia associated with progressive neural hearing loss.

Authors

No affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Case Reports
Journal Article
Research Support, U.S. Gov't, Non-P.H.S.

Language

eng

PubMed ID

890092

Citation

Jones, G, et al. "Familial Gingival Fibromatosis Associated With Progressive Deafness in Five Generations of a Family." Birth Defects Original Article Series, vol. 13, no. 3B, 1977, pp. 195-201.
Jones G, Wilroy RS, McHaney V. Familial gingival fibromatosis associated with progressive deafness in five generations of a family. Birth Defects Orig Artic Ser. 1977;13(3B):195-201.
Jones, G., Wilroy, R. S., & McHaney, V. (1977). Familial gingival fibromatosis associated with progressive deafness in five generations of a family. Birth Defects Original Article Series, 13(3B), 195-201.
Jones G, Wilroy RS, McHaney V. Familial Gingival Fibromatosis Associated With Progressive Deafness in Five Generations of a Family. Birth Defects Orig Artic Ser. 1977;13(3B):195-201. PubMed PMID: 890092.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Familial gingival fibromatosis associated with progressive deafness in five generations of a family. AU - Jones,G, AU - Wilroy,R S,Jr AU - McHaney,V, PY - 1977/1/1/pubmed PY - 2001/3/28/medline PY - 1977/1/1/entrez SP - 195 EP - 201 JF - Birth defects original article series JO - Birth Defects Orig Artic Ser VL - 13 IS - 3B N2 - Gingival hyperplasia may be inherited in a variety of ways, usually in an autosomal dominant or autosomal recessive manner. Additional phenotypic abnormalities are frequently associated with the gingival hyperplasia. To our knowledge, the family described here represents the first instance of autosomal dominantly inherited gingival hyperplasia associated with progressive neural hearing loss. SN - 0547-6844 UR - https://wwww.unboundmedicine.com/medline/citation/890092/Familial_gingival_fibromatosis_associated_with_progressive_deafness_in_five_generations_of_a_family_ L2 - https://www.diseaseinfosearch.org/result/2737 DB - PRIME DP - Unbound Medicine ER -