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Amyloidosis in a child with hyperimmunoglobulinemia D syndrome
Sibel Yel1, Zubeyde Gunduz, Funda Bastug
1Department of Pediatric Nephrology, Erciyes Medical University, Kayseri, Turkey. drsibelyel@gmail.com
Abstract:
Hereditary periodic fever syndromes are a group of genetic diseases clinically characterized by recurrent febrile attacks. Patients are at variable risks for the development of systemic reactive (AA) amyloidosis, leading to the nephrotic syndrome and kidney failure. We present the first report of the occurrence of renal AA amyloidosis causing severe nephrotic syndrome in a Turkish child affected with hyperimmunoglobulinemia D syndrome.
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