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PMID: 4061485 Published · ppublish English Journal Article

Muscular dystrophy in Saskatchewan Hutterites.

American journal of medical genetics ·Vol. 22 ·No. 3 ·1985-11-00 ·Pages 487-93

Shokeir MH, Rozdilsky B

Abstract

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.

MeSH Terms
Consanguinity Creatine Kinase/blood Electromyography Ethnicity Genetics, Population Humans Muscular Dystrophies/genetics,pathology,physiopathology Neural Conduction Pedigree Phenotype Religion Saskatchewan
Chemicals
Creatine Kinase
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Shokeir M H
Rozdilsky B
Article Info
Journal
American journal of medical genetics
Abbr.
Am J Med Genet
ISSN
0148-7299
Published
1985-11-00
Pages
487-93
Language
English
Region
United States
NLM ID
7708900
Subset
IM
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