Familial Mediterranean fever

Familial Mediterranean fever (FMF) is an autoinflammatory disorder characterized by recurrent short episodes of fever and serositis resulting in pain in the abdomen, chest, joints and muscles.

Glomerulopathy

Inflammatory or noninflammatory diseases affecting the glomeruli of the nephron.


Total: 2

                       


(per page)
PMID (PMCID)
12908875
(194618)
 MALE Middle Aged
Familial Mediterranean fever, inflammation and nephrotic syndrome: fibrillary glomerulopathy and the M680I missense mutation.
Fisher PW, Ho LT, Goldschmidt R, Semerdjian RJ, Rutecki GW.
BMC Nephrol. 2003;4:6.
Familial Mediterranean fever, inflammation and nephrotic syndrome: fibrillary glomerulopathy and the M680I missense mutation.
2609431
 MIXED_SAMPLE Infant, Newborn
The association of nephrotic syndrome and renal vein thrombosis: a clinicopathological analysis of eight pediatric patients.
Tinaztepe K, Buyan N, Tinaztepe B, Akkok N.
Turk J Pediatr. 1989;31(1):1-18.
The glomerulopathies of these nephrotic patients consisted of three cases of Finnish-type congenital NS (FCNS), three cases of renal amyloidosis secondary to familial Mediterranean fever, and two cases of membranoproliferative glomerulonephritis (MPGN).