Literature DB >> 3980016

A distinct dysmorphic syndrome with spinocerebellar ataxia and probable autosomal recessive inheritance.

J Sánchez-Corona, D García-Cruz, A González-Angulo, M C Alvarez-Arratia, R M Rodríguez, J M Cantú.   

Abstract

Two brothers and their sister aged 8, 13, and 7 years were found to have unusual facies (gross, rough and abundant hair, wide forehead, mild palpebral ptosis, small nose, anteverted nostrils, thick lips, and down-slanting corners of the mouth), dysarthria, delayed psychomotor development, scoliosis, feet deformities, and limb and gait ataxia. The characteristic clinical picture in the three sibs, once compared with other ataxic syndromes, allowed one to conclude that this could correspond to a distinct entity probably inherited as an autosomal recessive disorder.

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Year:  1985        PMID: 3980016     DOI: 10.1007/bf00293033

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  5 in total

1.  Cardiac aspects of Friedreich's ataxia.

Authors:  S H BOYER; A W CHISHOLM; V A McKUSICK
Journal:  Circulation       Date:  1962-03       Impact factor: 29.690

Review 2.  The olivopontocerebellar atrophies: a review.

Authors:  B W Konigsmark; L P Weiner
Journal:  Medicine (Baltimore)       Date:  1970-05       Impact factor: 1.889

3.  A linkage study of hereditary ataxias and related disorders. Evidence of heterogeneity of dominant cerebellar ataxia.

Authors:  L Pedersen; P Platz; L P Ryder; L U Lamm; J Dissing
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

4.  Heredoataxia (spinocerebellar degeneration), ERG alterations, temporal aspects.

Authors:  B Stanescu-Segal; J Michiels
Journal:  Ophthalmologica       Date:  1979       Impact factor: 3.250

5.  Hereditary ataxia in a large Danish pedigree.

Authors:  L Pedersen
Journal:  Clin Genet       Date:  1980-06       Impact factor: 4.438

  5 in total

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