Intractable & Rare Diseases Research
Case Reports
Lesch-Nyhan syndrome: The saga of metabolic abnormalities and self-injurious behavior
Nitesh TewariVijay Prakash MathurDivesh SardanaKalpana Bansal
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Volume 6 (2017) Issue 1 Pages 65-68

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Abstract

Lesch-Nyhan syndrome (LNS) is an X-linked recessive disorder of purine metabolism caused by a mutation in Xq26.2-q26.3 (OMIM 308000.0004). The presence of the diagnostic triad, i.e. signs of self-injurious behavior (SIB) and results of pedigree analysis and novel molecular biology & genetic testing, confirms the diagnosis of LNS. With a level of hypoxanthine guanine phosphoribosyl-transferase 1 (HPRT1) enzyme activity < 2%, patients develop neurological, neurocognitive, and neuromotor symptoms along with SIB. Described here is a case of 4-year-old boy who was diagnosed with LNS. The boy displayed SIB, i.e. biting of the lips and fingers, and he had cerebral venous sinus thrombosis caused by LNS.

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© 2017 International Research and Cooperation Association for Bio & Socio-Sciences Advancement
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