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Paper Information

Journal:   TEHRAN UNIVERSITY MEDICAL JOURNAL (TUMJ)   2004 , Volume 62 , Number 6; Page(s) 457 To 461.
 
Paper: 

ALLOPURINOL DESENSITIZATION IN LESCH- NYHAN SYNDROME (CASE REPORT)

 
 
Author(s):  OULIA M., HAGHIGHI A.
 
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Abstract: 

Lesch-Nyhan syndrome is one of the genetic disorders inherited as X-link mode. Its frequency is estimated to be one in every 100000 births. Severe deficiency of enzyme Hypoxanthine phosphoribosil transferase (HPRT) is the leading case of hyperuricemia, nephrolithiaisis, and devastating neurologic problems. Here we present a 30 year old man with chronic tophacious gout and multiple renal calculi since childhood. He had not tolerated the Allopurinol due to severe skin reactions. We claim this is the first reported case of allopurinol desensitization in Lesch-Nyhan syndrome.

 
Keyword(s): LESCH-NYHAN SYNDROME, GOUT, ALLOPURINOL HYPERSENSITIVITY
 
 
References: 
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Citations: 
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+ Click to Cite.
APA: Copy

OULIA, M., & HAGHIGHI, A. (2004). ALLOPURINOL DESENSITIZATION IN LESCH- NYHAN SYNDROME (CASE REPORT). TEHRAN UNIVERSITY MEDICAL JOURNAL (TUMJ), 62(6), 457-461. https://www.sid.ir/en/journal/ViewPaper.aspx?id=13389



Vancouver: Copy

OULIA M., HAGHIGHI A.. ALLOPURINOL DESENSITIZATION IN LESCH- NYHAN SYNDROME (CASE REPORT). TEHRAN UNIVERSITY MEDICAL JOURNAL (TUMJ). 2004 [cited 2021June17];62(6):457-461. Available from: https://www.sid.ir/en/journal/ViewPaper.aspx?id=13389



IEEE: Copy

OULIA, M., HAGHIGHI, A., 2004. ALLOPURINOL DESENSITIZATION IN LESCH- NYHAN SYNDROME (CASE REPORT). TEHRAN UNIVERSITY MEDICAL JOURNAL (TUMJ), [online] 62(6), pp.457-461. Available: https://www.sid.ir/en/journal/ViewPaper.aspx?id=13389.



 
 
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