Hyperimmunoglobulinemia D syndrome in an Arab child.

Abstract:

:Hyperimmunoglobulinemia D syndrome (HIDS) is newly recognized and resembles familial Mediterranean fever (FMF). It is inherited as an autosomal recessive trait. Mutation of the gene coding for mevalonate kinase is responsible for the disease. The gene is located at chromosome 12q24. The patients initially described were of Dutch ancestry. Other cases from Turkey and Armenia were reported. The case we present is the first from Arab countries to be registered in the International HIDS Registry and to our knowledge the first to be reported.

journal_name

Clin Rheumatol

journal_title

Clinical rheumatology

authors

Hammoudeh M

doi

10.1007/s10067-004-0953-0

subject

Has Abstract

pub_date

2005-02-01 00:00:00

pages

92-4

issue

1

eissn

0770-3198

issn

1434-9949

journal_volume

24

pub_type

信件
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