Lesch-Nyhan syndrome: The saga of metabolic abnormalities and self-injurious behavior

11Citations
Citations of this article
34Readers
Mendeley users who have this article in their library.

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.

Cite

CITATION STYLE

APA

Tewari, N., Mathur, V. P., Sardana, D., & Bansal, K. (2017). Lesch-Nyhan syndrome: The saga of metabolic abnormalities and self-injurious behavior. Intractable and Rare Diseases Research, 6(1), 65–68. https://doi.org/10.5582/irdr.2016.01076

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free