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Open Access 01-11-2013 | Meeting abstract

P01-041 – Patient management and rare FMF symptoms

Authors: MM Moradian, H Hayrapetyan, G Amaryan, A Yeghiazaryan, T Sarkisian

Published in: Pediatric Rheumatology | Special Issue 1/2013

Excerpt

Analysis of various symptoms from 20000 FMF patients indicates that several issues, including the clinical manifestation in a variety of combinations and the genotype penetrance, make FMF diagnosis and management challenging. Severe phenotypes with development of serositis, ELE, splenomegaly, and vasculitis are associated with high penetrance mutations of exon 10, mainly M694V allele. …

Title: P01-041 – Patient management and rare FMF symptoms
Authors: MM Moradian
H Hayrapetyan
G Amaryan
A Yeghiazaryan
T Sarkisian
Publication date: 01-11-2013
Publisher: BioMed Central
Published in: Pediatric Rheumatology / Issue Special Issue 1/2013
Electronic ISSN: 1546-0096
DOI: https://doi.org/10.1186/1546-0096-11-S1-A44

At a glance: The STEP trials

Springer Medicine

P01-041 – Patient management and rare FMF symptoms

Excerpt

At a glance: The STEP trials

Springer Medicine

Excerpt

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