A CASE OF LATE DIAGNOSIS OF FAMILIAL MEDITERRANEAN FEVER COMPLICATED BY AA-AMYLOIDOSIS

The aim of study was to describe a clinical case of a hereditary disease with autosomal recessive type of inheritance – familial Mediterranean fever (FMF).Materials and methods. Patient A., 19 years old, Armenian, was hospitalized in the Department of rheumatology of the clinical hospital with compl...

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Hlavní autoři: S. I. Shchadneva, E. E. Ustinova, L. V. Belozertseva, V. V. Gorbunov, N. S. Kurbatova
Médium: Artigo
Jazyk:Russo
Vydáno: ABV-press 2018-11-01
Edice:Klinicist
Témata:
recurrent disease
familial mediterranean fever
hereditary disease
aa-amyloidosis
difficult diagnosis of recurrent disease
nephrotic syndrome
nephrobiopsy
treatment of periodic disease
kidneys morphological study
colchicines
canakinumab
On-line přístup:https://klinitsist.abvpress.ru/Klin/article/view/355
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