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Lesch-Nyhan Syndrome in an Indian Child

Hypoxanthine guanine phosphoribosyl transferase-1 (HGPRT-1) leading to Lesch-Nyhan syndrome (LNS) is one of the important causes of self-mutilation. Hereby, we report a case of LNS in a three and half-year-old male child, who presented with characteristic self-mutilating behavior. He had history of...

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Autores principales: Chandekar, Priyanka, Madke, Bhushan, Kar, Sumit, Yadav, Nidhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4458947/
https://www.ncbi.nlm.nih.gov/pubmed/26120162
http://dx.doi.org/10.4103/0019-5154.156392
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author Chandekar, Priyanka
Madke, Bhushan
Kar, Sumit
Yadav, Nidhi
author_facet Chandekar, Priyanka
Madke, Bhushan
Kar, Sumit
Yadav, Nidhi
author_sort Chandekar, Priyanka
collection PubMed
description Hypoxanthine guanine phosphoribosyl transferase-1 (HGPRT-1) leading to Lesch-Nyhan syndrome (LNS) is one of the important causes of self-mutilation. Hereby, we report a case of LNS in a three and half-year-old male child, who presented with characteristic self-mutilating behavior. He had history of developmental delay, difficulty in social interaction, attention deficit and features of autism. His serum blood biochemistry was normal except for low hemoglobin levels and raised serum uric acid levels. With a diagnosis of LNS, the child was treated with allopurinol. With various modalities of physical restraint, his self-mutilating behavior came under control and currently the patient is being followed up.
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spelling pubmed-44589472015-06-26 Lesch-Nyhan Syndrome in an Indian Child Chandekar, Priyanka Madke, Bhushan Kar, Sumit Yadav, Nidhi Indian J Dermatol Case Report Hypoxanthine guanine phosphoribosyl transferase-1 (HGPRT-1) leading to Lesch-Nyhan syndrome (LNS) is one of the important causes of self-mutilation. Hereby, we report a case of LNS in a three and half-year-old male child, who presented with characteristic self-mutilating behavior. He had history of developmental delay, difficulty in social interaction, attention deficit and features of autism. His serum blood biochemistry was normal except for low hemoglobin levels and raised serum uric acid levels. With a diagnosis of LNS, the child was treated with allopurinol. With various modalities of physical restraint, his self-mutilating behavior came under control and currently the patient is being followed up. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4458947/ /pubmed/26120162 http://dx.doi.org/10.4103/0019-5154.156392 Text en Copyright: © Indian Journal of Dermatology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Chandekar, Priyanka
Madke, Bhushan
Kar, Sumit
Yadav, Nidhi
Lesch-Nyhan Syndrome in an Indian Child
title Lesch-Nyhan Syndrome in an Indian Child
title_full Lesch-Nyhan Syndrome in an Indian Child
title_fullStr Lesch-Nyhan Syndrome in an Indian Child
title_full_unstemmed Lesch-Nyhan Syndrome in an Indian Child
title_short Lesch-Nyhan Syndrome in an Indian Child
title_sort lesch-nyhan syndrome in an indian child
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4458947/
https://www.ncbi.nlm.nih.gov/pubmed/26120162
http://dx.doi.org/10.4103/0019-5154.156392
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