Progressive ataxia in Swedish children: a re-evaluation study.

Abstract:

:The results of follow-up of 76 children with progressive ataxia first reported in 1988 are described with special reference to type of potential underlying metabolic diseases. In 70% of cases the clinical follow-up did not lead to reconsideration of diagnoses. Six of 23 biochemically and morphologically re-examined children got a new and definite diagnosis: 1 myoclonic encephalopathy with ragged red fibres, 2 carbohydrate-deficient glycoprotein syndrome, 1 neuroborreliosis, 1 Hallervorden-Spatz disease and 1 leucodystrophy. Different clinical groups are discussed.

journal_name

Acta Neurol Scand

authors

Ylitalo V,Hagberg BA

doi

10.1111/j.1600-0404.1994.tb01684.x

subject

Has Abstract

pub_date

1994-04-01 00:00:00

pages

299-302

issue

4

eissn

0001-6314

issn

1600-0404

journal_volume

89

pub_type

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