Literature DB >> 154174

Huntington's chorea in a black Rhodesian family.

B L Samuels, M Gelfand.   

Abstract

Clinical features suggesting a diagnosis of Huntington's chorea in several siblings in a Black Rhodesian family are described. A progressive and eventually fatal mental deterioration accompanied by gradually worsening choreiform movements has until the present time occurred in only a single generation of this family, which precludes a definitive diagnosis based on the triad of family history, chorea and dementia. It is suggested that Huntington's chorea is the most likely diagnosis.

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Year:  1978        PMID: 154174

Source DB:  PubMed          Journal:  S Afr Med J


  6 in total

1.  Huntington disease in black African populations.

Authors:  E M Scrimgeour; S A Simpson
Journal:  Hum Genet       Date:  1992 Sep-Oct       Impact factor: 4.132

Review 2.  Epidemiology of neurodegenerative diseases in sub-Saharan Africa: a systematic review.

Authors:  Alain Lekoubou; Justin B Echouffo-Tcheugui; Andre P Kengne
Journal:  BMC Public Health       Date:  2014-06-26       Impact factor: 3.295

3.  Huntington disease in Maryland: clinical aspects of racial variation.

Authors:  S E Folstein; G A Chase; W E Wahl; A M McDonnell; M F Folstein
Journal:  Am J Hum Genet       Date:  1987-08       Impact factor: 11.025

4.  Huntington's disease in Tanzania.

Authors:  E M Scrimgeour
Journal:  J Med Genet       Date:  1981-06       Impact factor: 6.318

5.  Junctophilin 3 (JPH3) expansion mutations causing Huntington disease like 2 (HDL2) are common in South African patients with African ancestry and a Huntington disease phenotype.

Authors:  Amanda Krause; Claire Mitchell; Fahmida Essop; Susan Tager; James Temlett; Giovanni Stevanin; Christopher Ross; Dobrila Rudnicki; Russell Margolis
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2015-06-16       Impact factor: 3.568

6.  The high frequency of juvenile Huntington's chorea in South Africa.

Authors:  M R Hayden; J M MacGregor; D S Saffer; P H Beighton
Journal:  J Med Genet       Date:  1982-04       Impact factor: 6.318

  6 in total

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