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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
3
|
| pubmed:dateCreated |
1985-12-13
|
| pubmed:abstractText |
A slowly progressive form of muscular dystrophy was studied in a Dariusleut Hutterite kindred from a colony in west-central Saskatchewan. The disorder combines some characteristics of the dominantly inherited facio-scapulo-humeral and the recessively inherited limb-girdle types of muscular dystrophy. Intellect, vision, hearing, and sensations were normally preserved. Nerve conduction was also intact. The disorder reported herein resembles a type of muscular dystrophy we previously described in the Manitoba Schmiedeleut Hutterites [Shokeir and Kobrinsky, 1976]. This condition, which affects both sexes, appears to be genetic in origin and recessively inherited.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:month |
Nov
|
| pubmed:issn |
0148-7299
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
22
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
487-93
|
| pubmed:dateRevised |
2004-11-17
|
| pubmed:meshHeading |
pubmed-meshheading:4061485-Consanguinity,
pubmed-meshheading:4061485-Creatine Kinase,
pubmed-meshheading:4061485-Electromyography,
pubmed-meshheading:4061485-Ethnic Groups,
pubmed-meshheading:4061485-Genetics, Population,
pubmed-meshheading:4061485-Humans,
pubmed-meshheading:4061485-Muscular Dystrophies,
pubmed-meshheading:4061485-Neural Conduction,
pubmed-meshheading:4061485-Pedigree,
pubmed-meshheading:4061485-Phenotype,
pubmed-meshheading:4061485-Religion,
pubmed-meshheading:4061485-Saskatchewan
|
| pubmed:year |
1985
|
| pubmed:articleTitle |
Muscular dystrophy in Saskatchewan Hutterites.
|
| pubmed:publicationType |
Journal Article
|