Literature DB >> 10720116

Coeliac disease and Down syndrome: associations not due to genetic linkage on chromosome 21.

M A Morris1, J Y Yiannakou, A L King, P M Brett, F Biagi, R Vaughan, D Curtis, P J Ciclitira.   

Abstract

BACKGROUND: Individuals with Down syndrome have an increased prevalence of coeliac disease (CD). The HLA region accounts for only 30% of the heritability of CD, and segregation analyses have suggested the involvement of at least one other non-HLA gene. Distribution of known HLA susceptibility types in Down syndrome and normal populations are similar and do not explain the difference in disease frequency. This study tests the hypothesis that the association between these disorders is due to a susceptibility gene for coeliac disease being present on chromosome 21.
METHODS: We studied 21 families multiply affected with CD, none of whom had Down syndrome. The typing information of six microsatellite markers across chromosome 21 was used to test linkage.
RESULTS: Negative results from lod score and model-free linkage analysis were obtained, providing no support for genetic linkage of coeliac disease to chromosome 21 in this population.
CONCLUSIONS: The high prevalence of coeliac disease in Down syndrome is not due to an increased copy number of a polymorphic susceptibility gene on chromosome 21.

Entities:  

Mesh:

Year:  2000        PMID: 10720116     DOI: 10.1080/003655200750024353

Source DB:  PubMed          Journal:  Scand J Gastroenterol        ISSN: 0036-5521            Impact factor:   2.423


  2 in total

1.  Screening for celiac disease in Down's syndrome patients revealed cases of subtotal villous atrophy without typical for celiac disease HLA-DQ and tissue transglutaminase antibodies.

Authors:  Oivi Uibo; Kaupo Teesalu; Kaja Metskula; Tiia Reimand; Riste Saat; Tarvo Sillat; Koit Reimand; Tiina Talvik; Raivo Uibo
Journal:  World J Gastroenterol       Date:  2006-03-07       Impact factor: 5.742

2.  Psychosis and silent celiac disease in a down syndrome adolescent: a case report.

Authors:  Amparo Morant
Journal:  Case Rep Pediatr       Date:  2011-12-01
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.