Familial Mediterranean fever is inherited in an autosomal recessive manner. There are two
phenotypes: types 1 and 2. Familial Mediterranean fever type 1 is characterized by recurrent …

Neonatal-onset multisystem inflammatory disease (NOMID)/chronic infantile neurologic,
cutaneous, and arthritis (CINCA) syndrome is the most severe clinical phenotype in the …

The term autoinflammation was initially coined to distinguish disorders characterized by
recurrent episodes of inflammation in the absence of high-titer autoantibodies and antigen …

Familial Mediterranean fever (FMF) is a hereditary disorder characterised by recurrent
attacks of fever with peritonitis or pleuritis, arthritis, myalgia or erysipelas-like skin lesions …

Renal amyloidosis is a detrimental disease caused by the deposition of amyloid fibrils. A
child with renal amyloidosis may present with proteinuria or nephrotic syndrome. Chronic …

A host of clinical scenarios can be depicted in hereditary autoinflammatory diseases, and
the cardiovascular system can also be involved especially in familial Mediterranean fever …

AA amyloid patients who experience disease progression and develop renal failure have
not received sufficient benefit from agents that treat inflammation or infection. We have …

Familial Mediterranean fever (FMF) is a common hereditary autoinflammatory disorder
characterized by recurrent febrile attacks and polyserositis. The MEditerranean FeVer …

Background: A scarcity of data exists relating to the effect of amyloidosis of Familial
Mediterranean fever (FMF) on the autonomic nervous system. Our aim was to further …

Familial Mediterranean fever (FMF) is a hereditary disease, characterized by recurrent
episodes of fever and polyserositis. Heart rate variability (HRV) is a powerful, simple and …