Document Detail


DMPK-associated myotonic dystrophy and CTG repeats in Alabama African Americans.
MedLine Citation:
PMID:  17877752     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Myotonic dystrophy type 1 (DM1) is a result of a CTG expansion in the 3'-untranslated region of the DMPK gene. DM1 is rare among African blacks who have fewer large CTG repeats in the normal range than other racial/ethnic groups. Neither the prevalence of DM1 nor the relationship of CTG expansion to clinical status in African Americans (AAs) is well documented. We describe two AA brothers with DM1, each of whom had CTG repeats of 5/639; their father was reported to have DM1 and had CTG repeats of 5/60. Other family members had CTG repeats of 5-14. An unrelated AA patient from a second kinship also had DM1; an analysis revealed CTG repeats of 27/191. In 161 Alabama AA control subjects, we observed 18 CTG alleles from 5 to 28 repeats; the most common allele had five CTG repeats. The frequency of CTG repeats >or=15 were greater (p < 0.0003) in Pygmy, Amhara Ethiopian, Ashkenazi Jewish, North African Jewish, Israeli Muslim Arab, European white, and Japanese populations than in the Alabama AA population. These data suggest that the risk for DM1 in AAs is intermediate between that of African blacks and whites of European descent.
Authors:
R T Acton; C A Rivers; B Watson; S J Oh
Publication Detail:
Type:  Case Reports; Journal Article; Research Support, Non-U.S. Gov't     Date:  2007-09-17
Journal Detail:
Title:  Clinical genetics     Volume:  72     ISSN:  0009-9163     ISO Abbreviation:  Clin. Genet.     Publication Date:  2007 Nov 
Date Detail:
Created Date:  2007-10-15     Completed Date:  2008-01-04     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  0253664     Medline TA:  Clin Genet     Country:  Denmark    
Other Details:
Languages:  eng     Pagination:  448-53     Citation Subset:  IM    
Affiliation:
Department of Microbiology, University of Alabama, Birmingham, AL 35294-0005, USA. acton@uab.edu
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MeSH Terms
Descriptor/Qualifier:
Adult
African Americans / genetics*
Alabama
Female
Humans
Male
Middle Aged
Myotonic Dystrophy / genetics*
Pedigree
Protein-Serine-Threonine Kinases / genetics*
Trinucleotide Repeats*
Chemical
Reg. No./Substance:
EC 2.7.1.-/myotonic dystrophy protein kinase; EC 2.7.11.1/Protein-Serine-Threonine Kinases

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


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