Literature DB >> 4040696

Electrocochleographic changes in the hearing loss associated with X-linked hypophosphataemic osteomalacia.

S O'Malley, R T Ramsden, A Latif, R Kane, M Davies.   

Abstract

Transtympanic electrocochleography was carried out on 13 patients (21 ears) suffering from X-linked hypophosphataemic osteomalacia, and known to have cochlear hearing loss. The majority of ears exhibited a cochlear pattern of cochleogram with a recruiting input/output function and a markedly biphasic action potential. In addition 14 ears yielded a greatly enhanced negative summating potential, suggesting the presence of endolymphatic hydrops. It is proposed that the hearing loss so frequently associated with this condition is in part due to endolymphatic hydrops.

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Year:  1985        PMID: 4040696     DOI: 10.3109/00016488509108581

Source DB:  PubMed          Journal:  Acta Otolaryngol        ISSN: 0001-6489            Impact factor:   1.494


  7 in total

1.  Treatment of ear and bone disease in the Phex mouse mutant with dietary supplementation.

Authors:  Cameron C Wick; Sharon J Lin; Heping Yu; Cliff A Megerian; Qing Yin Zheng
Journal:  Am J Otolaryngol       Date:  2016-09-28       Impact factor: 1.808

2.  The Gy mutation: another cause of X-linked hypophosphatemia in mouse.

Authors:  M F Lyon; C R Scriver; L R Baker; H S Tenenhouse; J Kronick; S Mandla
Journal:  Proc Natl Acad Sci U S A       Date:  1986-07       Impact factor: 11.205

3.  New intragenic deletions in the Phex gene clarify X-linked hypophosphatemia-related abnormalities in mice.

Authors:  Bettina Lorenz-Depiereux; Victoria E Guido; Kenneth R Johnson; Qing Yin Zheng; Leona H Gagnon; Joiel D Bauschatz; Muriel T Davisson; Linda L Washburn; Leah Rae Donahue; Tim M Strom; Eva M Eicher
Journal:  Mamm Genome       Date:  2004-03       Impact factor: 2.957

4.  A Genetic Murine Model of Endolymphatic Hydrops: The Phex Mouse.

Authors:  Cameron C Wick; Maroun T Semaan; Qing Yin Zheng; Cliff A Megerian
Journal:  Curr Otorhinolaryngol Rep       Date:  2014-09

5.  Outcome of adult patients with X-linked hypophosphatemia caused by PHEX gene mutations.

Authors:  Douglas Chesher; Michael Oddy; Ulpee Darbar; Parag Sayal; Adrian Casey; Aidan Ryan; Annalisa Sechi; Charlotte Simister; Aoife Waters; Yehani Wedatilake; Robin H Lachmann; Elaine Murphy
Journal:  J Inherit Metab Dis       Date:  2018-02-19       Impact factor: 4.982

Review 6.  FGF23 and its role in X-linked hypophosphatemia-related morbidity.

Authors:  Signe Sparre Beck-Nielsen; Zulf Mughal; Dieter Haffner; Ola Nilsson; Elena Levtchenko; Gema Ariceta; Carmen de Lucas Collantes; Dirk Schnabel; Ravi Jandhyala; Outi Mäkitie
Journal:  Orphanet J Rare Dis       Date:  2019-02-26       Impact factor: 4.123

Review 7.  X-Linked Hypophosphatemic Rickets: Multisystemic Disorder in Children Requiring Multidisciplinary Management.

Authors:  Giampiero Igli Baroncelli; Stefano Mora
Journal:  Front Endocrinol (Lausanne)       Date:  2021-08-06       Impact factor: 5.555

  7 in total

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