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Case of purine nucleoside phosphorylase deficiency presented with hematuria
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作者 Saniye Girit Ferah Genel +2 位作者 Demet Can Mustafa Bak Michael Hershfield 《Open Journal of Pediatrics》 2012年第4期268-271,共4页
Purine Nucleoside Phosphorylase (PNP) deficiency is a rare autosomal recessive metabolic disorder. In PNP-deficiency disorder, the deficient enzyme leads to accumulation of toxic metabolites, especially in lymphocytes... Purine Nucleoside Phosphorylase (PNP) deficiency is a rare autosomal recessive metabolic disorder. In PNP-deficiency disorder, the deficient enzyme leads to accumulation of toxic metabolites, especially in lymphocytes and the metabolites exert toxic effect on T-cell generation. Purine nucleoside phosphorylase deficiency causes decreased numbers of T cells and lymphopenia. The patients suffering from PNP-deficiency may be admitted with recurrent infections, as well as neurological and autoimmune findings. We hereby presented a case admitted with the symptom of hematuria in which we established the diagnosis of PNP-deficiency early on the basis of detection of lymphopenia and low level of uric acid. 展开更多
关键词 PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY Infant HEMATURIA
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