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.

Leukopenia

An abnormal decreased number of leukocytes in the blood.


Total: 2

                       


(per page)
PMID (PMCID)
29240030
 FEMALE
A Case of Familial Mediterranean Fever Having Intermittent Leukopenia.
Beyitler I, Kavukcu S.
J Pediatr Hematol Oncol. 2018;40(2):e111-e112.
A Case of Familial Mediterranean Fever Having Intermittent Leukopenia.
17706281
 MALE Adult
Copper deficiency with increased hematogones mimicking refractory anemia with excess blasts.
Koca E, Buyukasik Y, Cetiner D, Yilmaz R, Sayinalp N, Yasavul U, Uner A.
Leuk Res. 2008;32(3):495-9.
We describe a 19-year-old male patient with a previous diagnosis of familial Mediterranean fever (FMF), nephrotic syndrome and secondary amyloidosis, who presented with anemia and leukopenia.