Progressive myopathy in trisomy 21.

Progressive myopathy in trisomy 21. Research Abstract Details 

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Progressive myopathy in trisomy 21. Abstract Text:

U Mielke,K Schimrigk,H Edlinger,U Mielke,K Schimrigk,H Edlinger,

A 23-year-old female patient with clinical manifestations typical of Down's syndrome progressively developed intensifying weakness of the proximal muscles from the age of 16 years. CK levels were distinctly elevated. Electromyography showed myogenic lesions and muscle biopsy a myopathic image with extensive fibre hypertrophy. Progressive sporadic myopathy in association with Down's syndrome has not been reported previously.

Progressive myopathy in trisomy 21. Publishing Authors By Initials

U Mielke,K Schimrigk,H Edlinger,U Mielke,K Schimrigk,H Edlinger,

For similar musculoskeletal diseases: muscular diseases research abstracts see: musculoskeletal diseases: muscular diseases research

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Progressive myopathy in trisomy 21. Journal Published:

PUBLICATION TYPE: Journal Article

Journal: Neuropediatrics

VOLUME: 19

Page Numbers: 132-4

Journal Abbreviation: Neuropediatrics

ISSN: 0174-304X

DAY: 16

MONTH: Aug

YEAR: 1988

Progressive myopathy in trisomy 21. Information

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LANGUAGE: eng

NlmUniqueID: 8101187

Progressive myopathy in trisomy 21. Keywords Mesh Terms:

KEYWORDS: Muscular Diseases

MESH TERMS: physiopathology

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Grant and Affiliation Information for Progressive myopathy in trisomy 21.

AFFILIATION: Department of Neurology, University of the Saarland, Homburg/Saar, FRG.

Country: GERMANY, WEST

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MEDLINETA: Neuropediatrics

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