Literature DB >> 2665489

Optic atrophy, hearing loss, and peripheral neuropathy.

K Hagemoser1, J Weinstein, G Bresnick, R Nellis, S Kirkpatrick, R M Pauli.   

Abstract

Here we report on two families with a previously apparently undescribed, autosomal dominant disorder resulting in optic atrophy and subsequent development of hearing loss and peripheral neuropathy. This disorder differs from previous syndromes resulting in this triad of effects both in the severity and early onset of the optic atrophy and in its mode of transmission. Review of published cases of optic atrophy + hearing loss + peripheral neuropathy suggests that there are at least three such specific disorders; classification of these published cases by first-appearing symptom also results in a clean division by most-likely inheritance.

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Year:  1989        PMID: 2665489     DOI: 10.1002/ajmg.1320330108

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


  4 in total

1.  Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss (CAPOS): a new syndrome.

Authors:  P Nicolaides; R E Appleton; A Fryer
Journal:  J Med Genet       Date:  1996-05       Impact factor: 6.318

2.  Autosomal dominant optic atrophy with asymptomatic peripheral neuropathy.

Authors:  R M Chalmers; A C Bird; A E Harding
Journal:  J Neurol Neurosurg Psychiatry       Date:  1996-02       Impact factor: 10.154

3.  Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene.

Authors:  H Eiberg; L Hansen; B Kjer; T Hansen; O Pedersen; M Bille; T Rosenberg; L Tranebjaerg
Journal:  J Med Genet       Date:  2006-05       Impact factor: 6.318

4.  Autosomal recessive inheritance of hereditary motor and sensory neuropathy with optic atrophy.

Authors:  R M Chalmers; P Riordan-Eva; N W Wood
Journal:  J Neurol Neurosurg Psychiatry       Date:  1997-04       Impact factor: 10.154

  4 in total

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