Document Detail


Autosomal dominant cramping disease.
MedLine Citation:
PMID:  2357164     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
A family was studied in which four generations (16 of 41 members) suffered from painful recurrent muscle cramping. A clear pattern of autosomal dominant inheritance was noted. The cramping first developed during adolescence or early adulthood. Electromyographic analysis indicated a neurogenic origin. The cramps seemed to be due to dysfunction of the motor neurons. The mechanisms underlying this alteration are unclear and require further investigation.
Authors:
K Ricker; R T Moxley
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  Archives of neurology     Volume:  47     ISSN:  0003-9942     ISO Abbreviation:  Arch. Neurol.     Publication Date:  1990 Jul 
Date Detail:
Created Date:  1990-07-24     Completed Date:  1990-07-24     Revised Date:  2007-11-14    
Medline Journal Info:
Nlm Unique ID:  0372436     Medline TA:  Arch Neurol     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  810-2     Citation Subset:  AIM; IM    
Affiliation:
Department of Neurology, University of Würzburg, West Germany.
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MeSH Terms
Descriptor/Qualifier:
Adolescent
Adult
Aged
Electromyography
Female
Humans
Leg
Male
Middle Aged
Muscle Cramp / genetics*
Pedigree
Grant Support
ID/Acronym/Agency:
AM-38193/AM/NIADDK NIH HHS; DK-32884/DK/NIDDK NIH HHS; RR-00044/RR/NCRR NIH HHS

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


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