Coexistence of Two Rare Genetic Disorders: Familial Mediterranean Fever and Neurofibromatosis Type 1 in A Child
Familial Mediterranean fever (FMF) is an autosomal recessive polysystemic disease characterized by attacks of relapsing and self-limiting fever, peritonitis, pleuritis and arthritis. Caf and eacute;-au lait macules, neurofibromas, axillary and inguinal freckling, Lisch nodules, bone lesions such as...
Main Authors: | , , , , , |
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Format: | Article |
Language: | English |
Published: |
Cukurova University
2015-03-01
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Series: | Çukurova Üniversitesi Tıp Fakültesi Dergisi |
Subjects: | |
Online Access: | http://www.scopemed.org/fulltextpdf.php?mno=184614 |