Literature DB >> 4050849

Facioscapulohumeral dystrophy with cochlear hearing loss and tortuosity of retinal vessels.

M A Gieron, J K Korthals, B G Kousseff.   

Abstract

We report on a mother and her three children with facioscapulohumeral dystrophy (FSHD), sensorineural hearing loss, and marked tortuosity of the retinal vessels. Initially the children presented with speech difficulties and hearing deficit. Hearing loss ranged from mild to severe. An audiologic evaluation, including brain stem auditory evoked responses in all patients, indicated a cochlear origin of hearing loss and intact pathways from the cochlea to the temporal lobe. The association of FSHD with hearing loss and tortuosity of the retinal vessels suggests previously unrecognized pleiotropy of FSHD (McKusick 15890) or a "new" type of FSHD.

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Year:  1985        PMID: 4050849     DOI: 10.1002/ajmg.1320220116

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  4 in total

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Authors:  Qian Liu; Takako Iida Jones; Vivian W Tang; William M Brieher; Peter L Jones
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3.  Dominant lethal pathologies in male mice engineered to contain an X-linked DUX4 transgene.

Authors:  Abhijit Dandapat; Darko Bosnakovski; Lynn M Hartweck; Robert W Arpke; Kristen A Baltgalvis; Derek Vang; June Baik; Radbod Darabi; Rita C R Perlingeiro; F Kent Hamra; Kalpna Gupta; Dawn A Lowe; Michael Kyba
Journal:  Cell Rep       Date:  2014-08-28       Impact factor: 9.423

4.  Facioscapulohumeral muscular dystrophy (FSHD) region gene 1 (FRG1) is a dynamic nuclear and sarcomeric protein.

Authors:  Meredith L Hanel; Chia-Yun Jessica Sun; Takako I Jones; Steven W Long; Simona Zanotti; Derek Milner; Peter L Jones
Journal:  Differentiation       Date:  2011-02       Impact factor: 3.880

  4 in total

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