Literature DB >> 2359100

Sex linked deafness: Wilde revisited.

W Reardon1.   

Abstract

Sex linked recessive deafness is a rare cause of male genetic deafness, estimated to account for 6.2% of male genetic deafness in 1966. A male excess was found in the deaf population of Ireland in 1851. Reevaluation of this survey of 1851 confirms sex linked deafness as a factor in the disproportionate number of deaf males and suggests that 5% of congenital male deafness was the result of sex linked recessive deafness. This study confirms that a small but constant proportion of male deafness is the result of sex linked recessive deafness. The figure derived is used to calculate an empirical risk for carrier status in female sibs of isolated cases of male deafness.

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Year:  1990        PMID: 2359100      PMCID: PMC1017135          DOI: 10.1136/jmg.27.6.376

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  7 in total

1.  Sex-linked hereditary deafness.

Authors:  J SATALOFF; P N PASTORE; E BLOOM
Journal:  Am J Hum Genet       Date:  1955-06       Impact factor: 11.025

2.  Sex-linked deafness of a possibly new type.

Authors:  J MOHR; K MAGEROY
Journal:  Acta Genet Stat Med       Date:  1960

3.  A note on deaf mutism.

Authors:  C S CHUNG; O W ROBINSON; N E MORTON
Journal:  Ann Hum Genet       Date:  1959-12       Impact factor: 1.670

4.  Congenital deafness due to a sex-linked recessive gene.

Authors:  N PARKER
Journal:  Am J Hum Genet       Date:  1958-06       Impact factor: 11.025

5.  The gene for X-linked progressive mixed deafness with perilymphatic gusher during stapes surgery (DFN3) is linked to PGK.

Authors:  H G Brunner; A van Bennekom; E M Lambermon; T L Oei; W R Cremers; B Wieringa; H H Ropers
Journal:  Hum Genet       Date:  1988-12       Impact factor: 4.132

6.  X-linked mixed deafness with stapes fixation in a Mauritian kindred: linkage to Xq probe pDP34.

Authors:  C Wallis; R Ballo; G Wallis; P Beighton; J Goldblatt
Journal:  Genomics       Date:  1988-11       Impact factor: 5.736

7.  Childhood deafness in the European community.

Authors:  J A Martin; O Bentzen; J R Colley; D Hennebert; C Holm; S Iurato; G A de Jonge; O McCullen; M L Meyer; W J Moore; A Morgon
Journal:  Scand Audiol       Date:  1981
  7 in total
  7 in total

Review 1.  Genetic deafness.

Authors:  W Reardon
Journal:  J Med Genet       Date:  1992-08       Impact factor: 6.318

2.  Deletion mapping of X-linked mixed deafness (DFN3) identifies a 265-525-kb region centromeric of DXS26.

Authors:  N Dahl; J Laporte; L Hu; V Biancalana; D Le Palier; D Cohen; C Piussan; J L Mandel
Journal:  Am J Hum Genet       Date:  1995-04       Impact factor: 11.025

3.  Loss-of-function mutations in the PRPS1 gene cause a type of nonsyndromic X-linked sensorineural deafness, DFN2.

Authors:  Xuezhong Liu; Dongyi Han; Jianzhong Li; Bing Han; Xiaomei Ouyang; Jing Cheng; Xu Li; Zhanguo Jin; Youqin Wang; Maria Bitner-Glindzicz; Xiangyin Kong; Heng Xu; Albena Kantardzhieva; Roland D Eavey; Christine E Seidman; Jonathan G Seidman; Li L Du; Zheng-Yi Chen; Pu Dai; Maikun Teng; Denise Yan; Huijun Yuan
Journal:  Am J Hum Genet       Date:  2010-01       Impact factor: 11.025

4.  Characterisation and genetic mapping of a new X linked deafness syndrome.

Authors:  D M Martin; F J Probst; S A Camper; E M Petty
Journal:  J Med Genet       Date:  2000-11       Impact factor: 6.318

5.  Cytoplasmic mislocalization of POU3F4 due to novel mutations leads to deafness in humans and mice.

Authors:  Thomas Parzefall; Shaked Shivatzki; Danielle R Lenz; Birgit Rathkolb; Kathy Ushakov; Daphne Karfunkel; Yisgav Shapira; Michael Wolf; Manuela Mohr; Eckhard Wolf; Sibylle Sabrautzki; Martin Hrabé de Angelis; Moshe Frydman; Zippora Brownstein; Karen B Avraham
Journal:  Hum Mutat       Date:  2013-05-08       Impact factor: 4.878

6.  [Clinical and molecular genetic analysis of monozygotic twins displaying stapes gusher syndrome (DFN3)].

Authors:  N Oh; S Kupka; F Mirghomizadeh; R Arold; R Zimmermann; N Blin; H P Zenner; M Pfister
Journal:  HNO       Date:  2003-04-11       Impact factor: 1.284

Review 7.  Hearing loss and PRPS1 mutations: Wide spectrum of phenotypes and potential therapy.

Authors:  Xue Zhong Liu; Dinghua Xie; Hui Jun Yuan; Arjan P M de Brouwer; John Christodoulou; Denise Yan
Journal:  Int J Audiol       Date:  2012-11-28       Impact factor: 2.117

  7 in total

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