Literature DB >> 15895791

Hereditary congenital unilateral deafness: a new disorder?

Frederik G Dikkers1, Joke B G M Verheij, Monique van Mechelen.   

Abstract

Congenital unilateral deafness is a rare disorder. The prevalence rates are unknown. The prevalence of children with severe to profound hearing losses that are congenital (or acquired before the development of speech and language) is 0.5 to 3 per 1,000 live births. Evidently, congenital unilateral deafness must have a lower prevalence. The purpose of this research was to present a new disorder, hereditary congenital unilateral deafness. A pedigree is presented in which both male and female members display symptoms of congenital unilateral deafness. Two affected persons and a normal-hearing member of the family have vestibular abnormalities without dysequilibrium. The inheritance pattern of this new syndrome is not clear. We hypothesize that the disorder might be new. A family like this has never before been presented in the medical literature.

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Year:  2005        PMID: 15895791     DOI: 10.1177/000348940511400414

Source DB:  PubMed          Journal:  Ann Otol Rhinol Laryngol        ISSN: 0003-4894            Impact factor:   1.547


  4 in total

1.  Unilateral hearing loss is associated with worse speech-language scores in children.

Authors:  Judith E C Lieu; Nancy Tye-Murray; Roanne K Karzon; Jay F Piccirillo
Journal:  Pediatrics       Date:  2010-05-10       Impact factor: 7.124

Review 2.  Asymmetric and unilateral hearing loss in children.

Authors:  Peter M Vila; Judith E C Lieu
Journal:  Cell Tissue Res       Date:  2015-05-26       Impact factor: 5.249

3.  Allelic Mutations of KITLG, Encoding KIT Ligand, Cause Asymmetric and Unilateral Hearing Loss and Waardenburg Syndrome Type 2.

Authors:  Celia Zazo Seco; Luciana Serrão de Castro; Josephine W van Nierop; Matías Morín; Shalini Jhangiani; Eva J J Verver; Margit Schraders; Nadine Maiwald; Mieke Wesdorp; Hanka Venselaar; Liesbeth Spruijt; Jaap Oostrik; Jeroen Schoots; Jeroen van Reeuwijk; Stefan H Lelieveld; Patrick L M Huygen; María Insenser; Ronald J C Admiraal; Ronald J E Pennings; Lies H Hoefsloot; Alejandro Arias-Vásquez; Joep de Ligt; Helger G Yntema; Joop H Jansen; Donna M Muzny; Gerwin Huls; Michelle M van Rossum; James R Lupski; Miguel Angel Moreno-Pelayo; Henricus P M Kunst; Hannie Kremer
Journal:  Am J Hum Genet       Date:  2015-10-29       Impact factor: 11.025

4.  4q27 deletion and 7q36.1 microduplication in a patient with multiple malformations and hearing loss: a case report.

Authors:  Maolan Wu; Xiangrong Zheng; Xia Wang; Guoyuan Zhang; Jian Kuang
Journal:  BMC Med Genomics       Date:  2020-03-03       Impact factor: 3.063

  4 in total

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