Literature DB >> 9929981

Autosomal dominant onychodystrophy and congenital sensorineural deafness.

T Kondoh1, A Tsuru, T Matsumoto, T Matsuzaka, Y Tsuji.   

Abstract

The disease "deafness and onychodystrophy" (DOD) is characterized by congenital hearing impairment and dystrophic or absent nails and teeth. The autosomal dominant form of the disorder has been previously reported only in one family. We describe here another family in which three members in three generations (a girl, her mother, and her maternal grandfather) were affected with DOD. Our finding is consistent with an autosomal dominant mode of inheritance and confirms autosomal dominant DOD (DDOD, MIM *124480) as a recognizable clinical entity.

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Year:  1999        PMID: 9929981     DOI: 10.1007/s100380050109

Source DB:  PubMed          Journal:  J Hum Genet        ISSN: 1434-5161            Impact factor:   3.172


  4 in total

1.  A Danish family with dominant deafness-onychodystrophy syndrome.

Authors:  Dina Vind-Kezunovic; Pernille M Torring
Journal:  J Dermatol Case Rep       Date:  2013-12-30

Review 2.  Hereditary Hearing Impairment with Cutaneous Abnormalities.

Authors:  Tung-Lin Lee; Pei-Hsuan Lin; Pei-Lung Chen; Jin-Bon Hong; Chen-Chi Wu
Journal:  Genes (Basel)       Date:  2020-12-30       Impact factor: 4.096

3.  Case Report: Exome Sequencing Identified Variants in Three Candidate Genes From Two Families With Hearing Loss, Onychodystrophy, and Epilepsy.

Authors:  Yuan Li; Jianjun Xiong; Yi Zhang; Lin Xu; Jianyun Liu; Tao Cai
Journal:  Front Genet       Date:  2021-11-29       Impact factor: 4.599

Review 4.  Genetic architecture and phenotypic landscape of deafness and onychodystrophy syndromes.

Authors:  Xue Gao; Pu Dai; Yong-Yi Yuan
Journal:  Hum Genet       Date:  2021-07-07       Impact factor: 4.132

  4 in total

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