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Early onset autosomal dominant spinocerebellar ataxia with miosis : Four cases

Timby, Niklas (author)
Umeå universitet,Pediatrik
Stattin, Eva-Lena (author)
Umeå universitet,Medicinsk och klinisk genetik
Kristiansen, Ingela (author)
Pediatric Clinic, Östersund Hospital, Sweden,Barnneurologi och barnonkologi
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Eriksson, Urban (author)
Pediatric Clinic, Östersund Hospital, Sweden
Erikson, Anders (author)
Umeå universitet,Pediatrik
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 (creator_code:org_t)
London : Saunders, 2008
2008
English.
In: European journal of paediatric neurology. - London : Saunders. - 1090-3798 .- 1532-2130. ; 12:1, s. 38-40
  • Journal article (other academic/artistic)
Abstract Subject headings
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  • Previously, at least 29 different forms of autosomal dominant spinocerebellar ataxias (SCAs) have been described. We describe a family with four members through three generations with autosomal dominant ataxia in combination with miosis and hyperreflexia. This family's ataxia does not match any of the previously described SCAs and is probably a novel form of SCA. To continue with the search for the genetic background of this disease, more cases are needed.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Pediatrik (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Pediatrics (hsv//eng)

Keyword

Spinocerebellar ataxia (SCA)
autosomal dominant
miosis
hyperreflexia
MEDICINE
MEDICIN
medicin
Medicine

Publication and Content Type

vet (subject category)
art (subject category)

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