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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
8
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pubmed:dateCreated |
2006-4-25
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pubmed:abstractText |
Hereditary spastic paraplegia (HSP) are classified clinically as pure when progressive spasticity occurs in isolation or complicated when other neurologic abnormalities are present. At least 22 genetic loci have been linked to HSP, 8 of which are autosomal recessive (ARHSP). HSP complicated with the presence of thin corpus callosum (HSP-TCC) is a common subtype of HSP. One genetic locus has been identified on chromosome 15q13-q15 (SPG11) for HSP-TCC, but some HSP-TCC families have not been linked to this locus.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
1526-632X
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pubmed:author |
pubmed-author:Al-BarwanyHH,
pubmed-author:Al-GazaliL ILI,
pubmed-author:Al-KindiMM,
pubmed-author:Al-YahyaeeSS,
pubmed-author:BayoumiR ARA,
pubmed-author:ChangWW,
pubmed-author:De JonghePP,
pubmed-author:De VriendtEE,
pubmed-author:GururajAA,
pubmed-author:JacobP CPC,
pubmed-author:KottMM,
pubmed-author:ParradoAA,
pubmed-author:SztrihaLL,
pubmed-author:Van BroeckhovenCC
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pubmed:issnType |
Electronic
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pubmed:day |
25
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pubmed:volume |
66
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1230-4
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:16636240-Asian Continental Ancestry Group,
pubmed-meshheading:16636240-Child,
pubmed-meshheading:16636240-Child, Preschool,
pubmed-meshheading:16636240-Chromosome Mapping,
pubmed-meshheading:16636240-Chromosomes, Human, Pair 8,
pubmed-meshheading:16636240-Corpus Callosum,
pubmed-meshheading:16636240-Epilepsy,
pubmed-meshheading:16636240-Genes, Recessive,
pubmed-meshheading:16636240-Genetic Linkage,
pubmed-meshheading:16636240-Genetic Markers,
pubmed-meshheading:16636240-Genotype,
pubmed-meshheading:16636240-Humans,
pubmed-meshheading:16636240-Intellectual Disability,
pubmed-meshheading:16636240-Spastic Paraplegia, Hereditary
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pubmed:year |
2006
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pubmed:articleTitle |
A novel locus for hereditary spastic paraplegia with thin corpus callosum and epilepsy.
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pubmed:affiliation |
College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Oman. syahyaee@squ.edu.om
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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