Fabry disease previously diagnosed as Henoch-Schonlein purpura

Henoch-Schonlein purpura (HSP) is a generalized vasculitis characterized by manifestations of the skin, joints, gastrointestinal tract, and renal involvement. Although HSP can occur at any age and is usually a self-limited disease in children, it is less common and has a poor prognosis in adults. Re...

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Veröffentlicht in:The Korean journal of internal medicine 2015, 30(6), , pp.925-927
Hauptverfasser: Kim, Ji Hyeong, Han, Dong Hoon, Park, Moo Yong, Choi, Soo Jeong, Kim, Jin Kuk, Hwang, Seung Duk, Jin, So Young
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Sprache:eng
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Zusammenfassung:Henoch-Schonlein purpura (HSP) is a generalized vasculitis characterized by manifestations of the skin, joints, gastrointestinal tract, and renal involvement. Although HSP can occur at any age and is usually a self-limited disease in children, it is less common and has a poor prognosis in adults. Renal involvement affects approximately one-third of HSP patients, and varies from intermittent hematuria and proteinuria, to severe nephrotic-nephritic syndrome with kidney histology being identical to that of immunoglobin A (IgA) nephropathy. KCI Citation Count: 2
ISSN:1226-3303
2005-6648
DOI:10.3904/kjim.2015.30.6.925