1. Familial Mediterranean Fever with Neonatal Onset: Case Report
- Author
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Serdar Umit Sarici, Demet Altun, Gonca Kolukisa, and Kübra Arslan
- Subjects
Abdominal pain ,Pediatrics ,medicine.medical_specialty ,Neonatal sepsis ,business.industry ,Familial Mediterranean fever ,Case Report ,General Medicine ,Neonatal onset ,medicine.disease ,Chest pain ,Occult ,RJ1-570 ,03 medical and health sciences ,0302 clinical medicine ,030225 pediatrics ,medicine ,Fever of unknown origin ,medicine.symptom ,business ,Serositis ,030217 neurology & neurosurgery - Abstract
Familial Mediterranean fever (FMF) is an autosomal recessively inherited disorder characterized by recurrent fever and attacks of abdominal pain, chest pain, and joint pain. Attacks of recurrent fever and serositis are encountered clinically. Attacks may present either with only one symptom or many simultaneous symptoms. Although most of the patients are diagnosed clinically above the age of 2, those cases who are diagnosed before 2 years of age and with clinical course of isolated fever are believed to have a more serious course and tend to develop amyloidosis. In this article, a case who was admitted first on the 22nd day of life and later diagnosed to have FMF with recurrent attacks of isolated fever and no other focus is presented. We emphasize that FMF may present as early as in the first month of life, and it should be considered in cases presenting with fever of unknown origin and misdiagnosed to have late neonatal sepsis or occult bacteremia at this age group.
- Published
- 2020