Literature DB >> 17497713

Familial unilateral deafness and delayed endolymphatic hydrops.

Kelley M Dodson1, Tamio Kamei, Aristides Sismanis, Walter E Nance.   

Abstract

Delayed endolymphatic hydrops (DEH) is a unique disorder characterized by fluctuating otologic symptoms in the setting of preexisting unilateral deafness. The symptoms include aural fullness, fluctuating hearing, and/or episodes of vertigo similar to those observed in Meniere disease and may occur ipsilateral or contralateral to the previously deafened ear. In most reported cases, the unilateral deafness has been a profound sensorineural hearing loss with a sudden onset that has been variously attributed to bacterial or viral labyrinthitis, acoustic or cranial trauma, otosclerosis, and congenital CMV infection. Familial occurrence of the syndrome has not previously been reported in the literature. In this report, we describe two possible familial instances of delayed DEH. These patients raise the possibility that genetic factors may sometimes be the cause of this unusual syndrome. (c) 2007 Wiley-Liss, Inc

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Year:  2007        PMID: 17497713     DOI: 10.1002/ajmg.a.31741

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  6 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

Review 3.  Vertigo and autoimmunity.

Authors:  Roberto Bovo; Andrea Ciorba; Alessandro Martini
Journal:  Eur Arch Otorhinolaryngol       Date:  2009-10-16       Impact factor: 2.503

4.  A mouse model with postnatal endolymphatic hydrops and hearing loss.

Authors:  Cliff A Megerian; Maroun T Semaan; Saba Aftab; Lauren B Kisley; Qing Yin Zheng; Karen S Pawlowski; Charles G Wright; Kumar N Alagramam
Journal:  Hear Res       Date:  2008-01-15       Impact factor: 3.208

5.  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

Review 6.  Update on Vertigo in Autoimmune Disorders, from Diagnosis to Treatment.

Authors:  Laura Girasoli; Diego Cazzador; Roberto Padoan; Ennio Nardello; Mara Felicetti; Elisabetta Zanoletti; Franco Schiavon; Roberto Bovo
Journal:  J Immunol Res       Date:  2018-09-26       Impact factor: 4.818

  6 in total

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