Literature DB >> 3180671

The petrous temporal bone and deafness in X-linked hypophosphataemic osteomalacia.

S P O'Malley1, J E Adams, M Davies, R T Ramsden.   

Abstract

Radiological anatomy of the petrous bones and skull base has been studied in a group of 11 patients with X-linked hypophosphataemic osteomalacia and hearing loss, and comparison made with a control group of normal subjects. Patients with X-linked hypophosphataemic osteomalacia were found to have generalised osteosclerosis and thickening of the petrous bone, with some narrowing of the internal auditory meatus, particularly in its mid-portion. No evidence of platybasia nor of basilar impression was found in the hypophosphataemmic group. The aetiology of the hearing loss which occurs in patients with X-linked hypophosphataemic osteomalacia is discussed in relation to the radiological abnormalities described.

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Year:  1988        PMID: 3180671     DOI: 10.1016/s0009-9260(88)80224-1

Source DB:  PubMed          Journal:  Clin Radiol        ISSN: 0009-9260            Impact factor:   2.350


  9 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.  Characterization of hearing-impairment in Generalized Arterial Calcification of Infancy (GACI).

Authors:  Elizabeth H Theng; Carmen C Brewer; Ralf Oheim; Christopher K Zalewski; Kelly A King; Maximillian M Delsmann; Tim Rolvien; Rachel I Gafni; Demetrios T Braddock; H Jeffrey Kim; Carlos R Ferreira
Journal:  Orphanet J Rare Dis       Date:  2022-07-19       Impact factor: 4.303

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.  Ectopic Mineralization and Conductive Hearing Loss in Enpp1asj Mutant Mice, a New Model for Otitis Media and Tympanosclerosis.

Authors:  Cong Tian; Belinda S Harris; Kenneth R Johnson
Journal:  PLoS One       Date:  2016-12-13       Impact factor: 3.240

6.  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 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

8.  Therapeutic management of hypophosphatemic rickets from infancy to adulthood.

Authors:  Agnès Linglart; Martin Biosse-Duplan; Karine Briot; Catherine Chaussain; Laure Esterle; Séverine Guillaume-Czitrom; Peter Kamenicky; Jerome Nevoux; Dominique Prié; Anya Rothenbuhler; Philippe Wicart; Pol Harvengt
Journal:  Endocr Connect       Date:  2014-03-14       Impact factor: 3.335

Review 9.  X-Linked Hypophosphatemia: A New Era in Management.

Authors:  Kathryn Dahir; Mary Scott Roberts; Stan Krolczyk; Jill H Simmons
Journal:  J Endocr Soc       Date:  2020-10-14
  9 in total

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