Please use this identifier to cite or link to this item:
Title: Familial CREST syndrome.
Austin Authors: McColl, G J;Buchanan, Russell R C 
Affiliation: Rheumatology
Medicine (University of Melbourne)
Issue Date: 1-Apr-1994
Publication information: The Journal of Rheumatology; 21(4): 754-6
Abstract: The familial occurrence of scleroderma is uncommon particularly the limited (CREST) form. We describe 2 families in which such an association occurred. Family pedigree 1 consists of 2 of 3 sisters with CREST scleroderma. Both affected sisters shared HLA types and C4 allotypes including DR5, found more frequently in patients with scleroderma. The unaffected sister did not share this MHC allele. Family pedigree 2 includes a grandmother and grandson with CREST scleroderma as well as a family member with Raynaud's phenomena alone. We conclude that familial occurrence of scleroderma may be associated with shared class II MHC antigens.
Type: Journal Article
Subjects: Adult
CREST Syndrome.genetics.immunology
Genetic Markers
HLA Antigens.genetics
HLA-DR5 Antigen.genetics
Appears in Collections:Journal articles

Show full item record

Page view(s)

checked on Dec 2, 2022

Google ScholarTM


Items in AHRO are protected by copyright, with all rights reserved, unless otherwise indicated.