Familial Mediterranean Fever: Diagnosing as Early as 3 Months of Age


Keskindemirci G. , Aktay A. , Aldemir E., Aydoğmuş C., Aydoğan G., Kavuncuoğlu S.

CASE REPORTS IN PEDIATRICS, 2014 (ESCI İndekslerine Giren Dergi) identifier identifier

  • Cilt numarası:
  • Basım Tarihi: 2014
  • Doi Numarası: 10.1155/2014/296479
  • Dergi Adı: CASE REPORTS IN PEDIATRICS

Özet

Familial Mediterranean Fever is an autosomal recessive disease. Major symptoms of disease are recurrent fever accompanied by serositis attacks. The disease is usually diagnosed before 20 years of age. Symptoms related to FMF are noted when children become more verbal, usually after 2 years of age. In this case report, the youngest patient with the diagnosis of FMF is presented. She was consulted to pediatric rheumatology for the high acute phase response and fever. It was learned that her mother had recurrent swelling of her ankle joints. Mutation analysis was performed and two homozygous mutations (M694V and R202Q) were identified. She was diagnosed as FMF at 3 months of age and colchicine was started. She responded to colchicine. Her uncontrolled acute phase response declined gradually. This case was reported to point out the importance of early remembrance of autoinflammatory diseases even at very early ages especially at endemic countries.