Heterogeneity of Wilson's Disease in Israel
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In a survey in Israel of 50 patients with Wilson's disease, it was found that this disease occurred in all ethnic groups. In the Arab patients there was a significantly early age of onset and the disease followed a more severe course than that in the Jewish patients. The overall sex ratio of patients was nearly 1:1, and genetic analysis of 20 families confirmed an autosomal recessive mode of inheritance. The very similar age of onset and type of disease within sibships and the varying ages of onset noted between the Arab and Jewish patients suggest that the disease is genetically heterogeneous.
Secondary athrocytotic cardiomyopathy--heart damage due to Wilson's disease.
Kaduk B, Metze K, Schmidt P, Brandt G Virchows Arch A Pathol Anat Histol. 1980; 387(1):67-80.
PMID: 7467117 DOI: 10.1007/BF00428430.
Assignment of the gene for Wilson disease to chromosome 13: linkage to the esterase D locus.
Frydman M, Bonne-Tamir B, Farrer L, Conneally P, Magazanik A, Ashbel S Proc Natl Acad Sci U S A. 1985; 82(6):1819-21.
PMID: 3856863 PMC: 397364. DOI: 10.1073/pnas.82.6.1819.
Mapping the Wilson disease locus to a cluster of linked polymorphic markers on chromosome 13.
Bowcock A, Farrer L, Cavalli-Sforza L, Hebert J, Kidd K, Frydman M Am J Hum Genet. 1987; 41(1):27-35.
PMID: 3474893 PMC: 1684171.
Farrer L, Bonne-Tamir B, Frydman M, Magazanik A, Kidd K, Bowcock A Hum Genet. 1988; 79(2):109-17.
PMID: 3164701 DOI: 10.1007/BF00280547.
Linkage of the Wilson disease gene to chromosome 13 in North-American pedigrees.
Yuzbasiyan-Gurkan V, Brewer G, Boerwinkle E, Venta P Am J Hum Genet. 1988; 42(6):825-9.
PMID: 3163469 PMC: 1715195.