Literature DB >> 3992413

Myotonic dystrophy. Part I. A genealogical study in the northern Transvaal.

B P Lotz, C H van der Meyden.   

Abstract

Myotonic dystrophy is a disabling multisystem disorder which appears to be more common in South Africa than is generally recognized. Twenty white kindreds with the disease were studied; of these 4 large kindreds had a common ancestry. Genealogical data for 1 527 individuals were acquired. The minimum prevalence of myotonic dystrophy in the northern Transvaal was found to be 14,3/100 000 of the population. Recognition of the disorder is important since some of its complications are preventable and others potentially treatable.

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Year:  1985        PMID: 3992413

Source DB:  PubMed          Journal:  S Afr Med J


  6 in total

Review 1.  Medical genetics in South Africa.

Authors:  T Jenkins
Journal:  J Med Genet       Date:  1990-12       Impact factor: 6.318

Review 2.  Myotonic dystrophy.

Authors:  Charles A Thornton
Journal:  Neurol Clin       Date:  2014-06-06       Impact factor: 3.806

3.  Founder effect and prevalence of myotonic dystrophy in South Africans: molecular studies.

Authors:  A Goldman; A Krause; M Ramsay; T Jenkins
Journal:  Am J Hum Genet       Date:  1996-08       Impact factor: 11.025

4.  Absence of myotonic dystrophy in southern African Negroids is associated with a significantly lower number of CTG trinucleotide repeats.

Authors:  A Goldman; M Ramsay; T Jenkins
Journal:  J Med Genet       Date:  1994-01       Impact factor: 6.318

5.  New founder haplotypes at the myotonic dystrophy locus in southern Africa.

Authors:  A Goldman; M Ramsay; T Jenkins
Journal:  Am J Hum Genet       Date:  1995-06       Impact factor: 11.025

6.  Presymptomatic diagnosis of myotonic dystrophy.

Authors:  H G Brunner; W Nillesen; B A van Oost; G Jansen; B Wieringa; H H Ropers; H J Smeets
Journal:  J Med Genet       Date:  1992-11       Impact factor: 6.318

  6 in total

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