AA amyloidosis as a rare presentation leading to the diagnosis of mevalonate kinase deficiency in a male adult: a diagnostic challenge mimicking familial Mediterranean fever.

IF 3.2 4区医学 Q2 RHEUMATOLOGY

Clinical and experimental rheumatology Pub Date : 2026-10-09 DOI:10.55563/clinexprheumatol/0rs4nj

Alba Chiara Pozzi, Giulia Voltarel, Paolo Airo', Micol Frassi, Ilaria Cavazzana, Francesca Crisafulli

引用次数: 0

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AA淀粉样变作为一种罕见的表现，导致男性成人甲羟戊酸激酶缺乏症的诊断：一个模拟家族性地中海热的诊断挑战。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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来源期刊

Clinical and experimental rheumatology 医学-风湿病学

CiteScore

6.10

自引率

18.90%

发文量

377

审稿时长

3-6 weeks

期刊介绍： Clinical and Experimental Rheumatology is a bi-monthly international peer-reviewed journal which has been covering all clinical, experimental and translational aspects of musculoskeletal, arthritic and connective tissue diseases since 1983.