Child's urinary lithiasis revealing a complete deficit in adenine phosphoribosyl transferase.
作者信息
Debray H, Cartier P, Temstet A, Cendron J
出版信息
Pediatr Res. 1976 Aug;10(8):762-6. doi: 10.1203/00006450-197608000-00014.
PMID:7766
Abstract
In one case of a urinary lithiasis, termed "uric lithiasis" on biochemical examination, the authors describe the symptomatology of a child with a complete deficit in adenine phosphoribosyl transferase. After more intensive investigation the calculi have been found to be composed of a new clinical compound: 2,8-hydroxyadenine.
摘要
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