Literature DB >> 1661780

Two sisters with mental retardation, cataract, ataxia, progressive hearing loss, and polyneuropathy.

J H Begeer1, F A Scholte, A J van Essen.   

Abstract

Two sisters are described with a disorder characterised by mental retardation, congenital cataract, progressive spinocerebellar ataxia, sensorineural deafness, and signs of peripheral neuropathy. Progressive hearing loss, ataxia, and polyneuropathy became evident in the third decade. The differential diagnosis of this syndrome is discussed including the syndromes described by Berman et al and Koletzko et al.

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Year:  1991        PMID: 1661780      PMCID: PMC1017170          DOI: 10.1136/jmg.28.12.884

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


  6 in total

1.  [FAMILIAL SYNDROME COMBINING ATAXIA, DEAFNESS AND OLIGOPHRENIA. MYOCARDIAL SCLEROSIS WITH FATAL DEVELOPMENT IN ONE OF THE CHILDREN].

Authors:  M JEUNE; M TOMMASI; F FREYCON; J L NIVELON
Journal:  Pediatrie       Date:  1963

2.  A new familial syndrome with ataxia, hearing loss, and mental retardation. Report of three brothers.

Authors:  W Berman; R H Haslam; B W Koningsmark; A J Capute; C J Migeon
Journal:  Arch Neurol       Date:  1973-10

3.  Cataract, deafness, cerebellar ataxia, psychosis and dementia--a new syndrome.

Authors:  E Strömgren; A Dalby; M A Dalby; B Ranheim
Journal:  Acta Neurol Scand       Date:  1970       Impact factor: 3.209

4.  Hereditary congenital spinocerebellar ataxia accompanied by congenital cataract and oligophrenia; a genetic and clinical investigation.

Authors:  T SJOGREN
Journal:  Confin Neurol       Date:  1950

5.  A neuroectodermal syndrome of dominant inheritance.

Authors:  P Flynn; R B Aird
Journal:  J Neurol Sci       Date:  1965 Mar-Apr       Impact factor: 3.181

6.  Ataxia-deafness-retardation syndrome in three sisters.

Authors:  S Koletzko; B Koletzko; A Lamprecht; H G Lenard
Journal:  Neuropediatrics       Date:  1987-02       Impact factor: 1.947

  6 in total

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