Familial Mediterranean fever (FMF) is a hereditary epidosic febrile syndrome that is
expressed by acute spells of fever, painful manifestations in the abdomen, chest and joints …

Familial Mediterranean fever (FMF) is the most prevalent type of hereditary recurrent fever.
Although the inflammatory attacks that characterize the disease may sometimes be …

Objective To present an overview of the published data on endocrine involvement and
endocrine dysfunction in patients with systemic amyloidosis. Methods We conducted a …

This study comprised 74 infertile patients with familial Mediterranean fever (FMF), among
which 26 women became pregnant. Pregnancies were followed according to the standard …

Familial Mediterranean Fever (FMF) or recurrent polyserositis is an inherited multisystem
disease manifested by recurrent painful attacks affecting the abdomen, chest or joints, often …

Our aim was to describe the main features of amyloid goiter in adults with amyloidosis
secondary to familial Mediterranean fever. Therefore, we analyzed cases from a French …

Ailevi Akdeniz ateşi (FMF), rekurrent febril epizodlar ve seröz membranların inflamasyonu ile
karakterize genetik bir hastalıktır. Akdeniz kökenli etnik gruplarda sık görülmektedir …

In Turkey, familial Mediterranean fever (FMF) is an important cause of nephrotic syndrome
and endstage renal disease due to renal deposition of AA type amyloid. We report a case of …

We describe a case of amyloid goiter revealing a systemic amyloidosis secondary to familial
Mediterranean fever (FMF) with homozygous MEFV mutation, and we review the literature. A …

Systemic infiltrative diseases are relatively rare conditions consisting of cell infiltration or
substance deposition in multiple organs and systems, including endocrine glands. This …