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Article

Overlap of familial Mediterranean fever and hyper-IgD syndrome in an Arabic kindred.

Journal of clinical immunology - 1 Apr 2015

Moussa Taha, Aladbe Buthaina, Taha Rowaida Z, Remmers Elaine F, El-Shanti Hatem, Fathalla Basil M

Abstract excerpt

Hyperimmunoglobulinemia D Syndrome (HIDS) has rarely been reported in Arabs. Moreover, the simultaneous presence of mutations in MEFV and MVK segregating in the same family is exceptional. We report an Arabic girl presenting since the age of 8-years with two patterns of recurrent episodes of fever, and associated with a spectrum of clinical features suggestive of overlap between familial Mediterranean fever (FMF)...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 25708585
DOI: 10.1007/s10875-015-0140-x

Genes

MEFV
MVK

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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