- ABSTRACT Page 1 859 Familial Mediterranean Fever and Primary Antiphospholipid
Syndrome, a Rare Association A Case Report Jose Halabe-Cherem, MD, FACP Haiko …

Two patients with familial Mediterranean fever showed the classic features of pericardial
involvement and one of them (Case 2) had pericardial effusion detected by …

Familial Mediterranean fever (FMF) is the autoinflammatorydisease and hereditary periodic
fever syndrome that most commonly affects people of Eastern Mediterranean origin. It is …

We report a rare case of a patient with long-standing familial Mediterranean fever who
presented with sudden onset of dyspnea, abdominal pain, and cutaneous manifestations …

We describe a 14-year-old boy with a 5-year history of familial Mediterranean fever (FMF),
treated with colchicine, who developed polyarteritis nodosa (PAN). He was admitted to our …

Familial Mediterranean fever (FMF) is an ethnicity-specific autoinflammatory disease
prevalent in the Arab world. It has various presentations including amyloidosis, small-vessel …

A 16-year-old girl, presenting initially with pericarditis and life threatening pericardial
tamponade, developed clinical episodes characteristic of FMF few months later. This case …

We reported here on three patients in whom the diagnosis of familial Mediterranean fever
was established after avascular necrosis of the femoral head had been detected. The …

A perirenal haematoma, associated with the presence of renal micro-aneurysms, developed
in three patients with periodic syndrome. In one of the cases, the histology of a …

The diagnosis of familial Mediterranean fever (FMF) is based on clinical evidence, since
there is no specific diagnostic test. Manifestations are recurrent attacks of fever …