Document Detail


A family study of coeliac disease.
MedLine Citation:
PMID:  1121023     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Thirteen of 141 cases (9 percent) of overt, biopsy proven coeliac disease had a definitely affected relative. The pattern of inheritance in these families is compatible with an incompletely penetrant autosomal dominant gene. There was a female preponderance in the adults and the sporadic cases, but not in the children or the familial cases. The series included a pair of concordant and probably monozygotic twins. The authors believe that coeliac disease, as defined at present, is a heterogeneous condition.
Authors:
T J David; A B Ajdukiewicz
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Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Journal of medical genetics     Volume:  12     ISSN:  0022-2593     ISO Abbreviation:  J. Med. Genet.     Publication Date:  1975 Mar 
Date Detail:
Created Date:  1975-06-25     Completed Date:  1975-06-25     Revised Date:  2009-11-19    
Medline Journal Info:
Nlm Unique ID:  2985087R     Medline TA:  J Med Genet     Country:  ENGLAND    
Other Details:
Languages:  eng     Pagination:  79-82     Citation Subset:  IM    
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MeSH Terms
Descriptor/Qualifier:
Adolescent
Adult
Biopsy
Celiac Disease / genetics*
Child
Diseases in Twins
Female
Gene Frequency
Genes, Dominant
Genetic Variation
Humans
Jejunum / pathology
Male
Pedigree
Phenotype
Selection, Genetic
Sex Factors
Comments/Corrections

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