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. 2020 Nov 3;50(7):1591–1610. doi: 10.3906/sag-2008-11

Table 2.

Differential diagnoses of familial Mediterranean fever.

Mevalonate kinase deficiency (MKD) Inflammatory bowel disease
TNF receptor-associated periodic syndrome (TRAPS) Porphyria
Periodic fever, aphthous stomatitis, pharyngitis, and adenopathy (PFAPA) Median arcuate ligament syndrome
Hereditary angioedema Intestinal adhesion
Fabry disease Adrenal failure
Cyclic neutropenia Chronic recurrent infections
Yao syndrome Mesothelioma