Erschienen in:
01.11.2007 | Brief Report
Rare variant of Lesch–Nyhan syndrome without self-mutilation or nephrolithiasis
verfasst von:
Tanja Kersnik Levart
Erschienen in:
Pediatric Nephrology
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Ausgabe 11/2007
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Abstract
Lesch–Nyhan syndrome is a very rare X-linked recessive disorder characterized by mental retardation, spasticity resembling cerebral palsy, choreo-athetosis, self-mutilation and hyperuricemia. Self-mutilative behavior is a hallmark of the disease. Hyperuricemia leads to hyperuricuria and uric acid nephrolithiasis. The underlying defect is a deficiency of hypoxanthine-guanine-phosphoribosyl transferase. We report on a 7-year-old boy with Lesch–Nyhan syndrome, lacking self-mutilative behavior, who was erroneously diagnosed as having athetotic cerebral palsy. He also had no renal stones; hyperechoic renal medullary pyramids were the only renal abnormality detected and were sonographically indistinguishable from medullary nephrocalcinosis.