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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
4
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pubmed:dateCreated |
2008-4-3
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pubmed:abstractText |
Myoclonus-dystonia (M-D) due to SGCE mutations is characterized by early onset myoclonic jerks, often associated with dystonia. Penetrance is influenced by parental sex, but other sex effects have not been established. In 42 affected individuals from 11 families with identified mutations, we found that sex was highly associated with age at onset regardless of mutation type; the median age onset for girls was 5 years versus 8 years for boys (P < 0.0097). We found no association between mutation type and phenotype.
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pubmed:grant |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
1531-8257
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pubmed:author |
pubmed-author:BressmanSusanS,
pubmed-author:BrinMitchell FMF,
pubmed-author:DohenyDanaD,
pubmed-author:FordBlairB,
pubmed-author:FriedmanJenniferJ,
pubmed-author:FruchtStevenS,
pubmed-author:HarrisJulietteJ,
pubmed-author:HeimanGary AGA,
pubmed-author:JenningsDannaD,
pubmed-author:KleinChristineC,
pubmed-author:KockNormanN,
pubmed-author:KurlanRogerR,
pubmed-author:LangAnthony EAE,
pubmed-author:Multhaupt-BuellTrishaT,
pubmed-author:OzeliusLaurieL,
pubmed-author:RaymondDeborahD,
pubmed-author:Saunders-PullmanRachelR,
pubmed-author:SchuleBirgittB,
pubmed-author:de Carvalho AguiarPatriciaP,
pubmed-author:de Leon BrinDeborahD
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pubmed:copyrightInfo |
(c) 2007 Movement Disorder Society.
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pubmed:issnType |
Electronic
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pubmed:day |
15
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pubmed:volume |
23
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
588-92
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pubmed:meshHeading |
pubmed-meshheading:18175340-Adult,
pubmed-meshheading:18175340-Aged,
pubmed-meshheading:18175340-DNA Mutational Analysis,
pubmed-meshheading:18175340-Dystonia,
pubmed-meshheading:18175340-Exons,
pubmed-meshheading:18175340-Female,
pubmed-meshheading:18175340-Humans,
pubmed-meshheading:18175340-Introns,
pubmed-meshheading:18175340-Male,
pubmed-meshheading:18175340-Myoclonus,
pubmed-meshheading:18175340-Phenotype,
pubmed-meshheading:18175340-Point Mutation,
pubmed-meshheading:18175340-Sarcoglycans,
pubmed-meshheading:18175340-Severity of Illness Index,
pubmed-meshheading:18175340-Sex Factors
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pubmed:year |
2008
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pubmed:articleTitle |
Phenotypic spectrum and sex effects in eleven myoclonus-dystonia families with epsilon-sarcoglycan mutations.
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pubmed:affiliation |
The Alan and Barbara Mirken Department of Neurology, Beth Israel Medical Center, New York, New York 10003, USA.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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