Document Detail


Neonatal rhabdomyolysis as a presentation of muscular dystrophy.
MedLine Citation:
PMID:  3399077     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
We report a unique presentation of X-linked recessive dystrophy as neonatal rhabdomyolysis. There was induration of the proximal musculature in an otherwise well neonate and striking CK elevation, without myoglobinuria. Muscle biopsy at age 1 year showed dystrophic alterations, and X chromosome analysis showed a deletion within or adjacent to the Duchenne/Becker locus.
Authors:
G N Breningstall; W D Grover; S Barbera; H G Marks
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Neurology     Volume:  38     ISSN:  0028-3878     ISO Abbreviation:  Neurology     Publication Date:  1988 Aug 
Date Detail:
Created Date:  1988-08-30     Completed Date:  1988-08-30     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  0401060     Medline TA:  Neurology     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  1271-2     Citation Subset:  AIM; IM    
Affiliation:
Department of Pediatrics, St. Christopher's Hospital for Children, Philadelphia, PA.
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MeSH Terms
Descriptor/Qualifier:
Creatine Kinase / blood
Humans
Infant, Newborn
Male
Muscular Dystrophies / complications*,  enzymology
Rhabdomyolysis / complications*,  enzymology
Chemical
Reg. No./Substance:
EC 2.7.3.2/Creatine Kinase

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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