Literature DB >> 894124

Sensorineural deafness associated with recessive hypophosphataemic rickets.

N Weir.   

Abstract

Two pairs of siblings suffering from recessive hypophosphataemic rickets are presented, three members of which have some degree of sensorineural deafness and all of which have bilateral marked narrowing of the internal auditory canals. The biochemical explanation of the condition is discussed.

Entities:  

Mesh：

Year:  1977        PMID： 894124     DOI： 10.1017/s0022215100084255

Source DB:  PubMed          Journal:  J Laryngol Otol        ISSN： 0022-2151            Impact factor:   1.469


  11 in total

Review 1.  Hearing impairment in familial X-linked hypophosphatemic rickets.

Authors:  Gadi Fishman; Denise Miller-Hansen; Cynthia Jacobsen; Virender K Singhal; Uri S Alon
Journal:  Eur J Pediatr       Date:  2004-10       Impact factor: 3.183

2.  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

3.  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

4.  Vitamin D deficiency and deafness.

Authors:  E B Brookes; A W Morrison
Journal:  Br Med J (Clin Res Ed)       Date:  1981-07-25

5.  A novel auditory ossicles membrane and the development of conductive hearing loss in Dmp1-null mice.

Authors:  Kun Lv; Haiyang Huang; Xing Yi; Mark E Chertoff; Chaoyuan Li; Baozhi Yuan; Robert J Hinton; Jian Q Feng
Journal:  Bone       Date:  2017-06-08       Impact factor: 4.398

6.  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

7.  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

8.  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

9.  Prevalence of Hearing Disorders among Type 2 Diabetes Mellitus Patients with and without Vitamin D Deficiency.

Authors:  Mahbobeh Sadat Hosseini; Masoumeh Saeedi; Seyed Alireza KHALKHALi
Journal:  Maedica (Bucur)       Date:  2020-03

10.  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
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.