Journals / Türk Pediatri Arşivi / 1993 / Cilt: 28 Sayı: 4

A Case of Lesch Nyhan Syndrome

Bir Lesch Nyhan Sendromu Olgusu

Pages
1–1
Publication Date
1993-12-01
DOI
—
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⚡ TL;DR(Too Long; Didn't Read)

Lesch Nayhan syndrome is a rare X linked recessive disorder of purine metabolism due to the severe deficiency of the enzyme hypoxanthine guanin phosphoribosyl transferase The disease is characterized by hyperuricemia self mutilation choreathetosis spasticity and mental retardation In this paper a case of Lesch Nyhan syndrome with mental retardation spasticity self mutilation is presented and relevant literature is reviewed Key words: Lesch Nyhan Syndrome Self Mutilation Purine Metabolism

📌 3 Key Takeaways

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Objective & Hypothesis:Lesch Nayhan syndrome is a rare X linked recessive disorder of purine metabolism due to the severe deficiency of the enzyme hypoxanthine guanin phosphoribosyl transferase The disease is characterized by hyperuricemia self mutilation choreathetosis spasticity and mental retardation In this paper a case of Lesch Nyhan syndrome with mental retardation spasticity self mutilation is presented and relevant literature is reviewed Key words: Lesch Nyhan Syndrome Self Mutilation Purine Metabolism
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Key Findings & Data:Lesch Nayhan syndrome is a rare X linked recessive disorder of purine metabolism due to the severe deficiency of the enzyme hypoxanthine guanin phosphoribosyl transferase The disease is characterized by hyperuricemia self mutilation choreathetosis spasticity and mental retardation In this paper a case of Lesch Nyhan syndrome with mental retardation spasticity self mutilation is presented and relevant literature is reviewed Key words: Lesch Nyhan Syndrome Self Mutilation Purine Metabolism
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Conclusion & Impact:Lesch Nayhan syndrome is a rare X linked recessive disorder of purine metabolism due to the severe deficiency of the enzyme hypoxanthine guanin phosphoribosyl transferase The disease is characterized by hyperuricemia self mutilation choreathetosis spasticity and mental retardation In this paper a case of Lesch Nyhan syndrome with mental retardation spasticity self mutilation is presented and relevant literature is reviewed Key words: Lesch Nyhan Syndrome Self Mutilation Purine Metabolism
🔬Design:Review & Systematic Survey
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Lesch Nayhan syndrome is a rare X linked recessive disorder of purine metabolism due to the severe deficiency of the enzyme hypoxanthine guanin phosphoribosyl transferase The disease is characterized by hyperuricemia self mutilation choreathetosis spasticity and mental retardation In this paper a case of Lesch Nyhan syndrome with mental retardation spasticity self mutilation is presented and relevant literature is reviewed Key words: Lesch Nyhan Syndrome Self Mutilation Purine Metabolism

Özet

Lesch Nyhan sendromu purin metabolizmasının X e bağlı resesif kalıtılan bir bozukluğudur Bozukluğun sebebi hipoksantin guanin fosforibozil transferaz enziminin eksikliğidir Hastalıkta hiperürisemi selfmutilasyon koreoatetosis spastisite ve mental retardasyon ile karakterizedir Bu yazıda mental retardasyonu selfmütilasyonu spastisitesi olan bir Lesch Nyhan sendromu olgusu ve ilgili literatür gözden geçirildi Anahtar kelimeler: Lesch Nyhan Sendromu Selfmutilasyon Purin Metabolizması

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Cite This Article

Toksoy, H. B., Tanzer, F., İçağasıoğlu, D., Kafalı, G., Ergür, A. T. (1993). A Case of Lesch Nyhan Syndrome. Türk Pediatri Arşivi, Cilt: 28 Sayı: 4, 1–1. https://ajindex.com/articles/1012506

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