Journal of South Asian Federation of Obstetrics and Gynaecology

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VOLUME 5 , ISSUE 1 ( January-April, 2013 ) > List of Articles

CASE REPORT

A Case of Mucopolysaccharidosis II /I-Cell Disease

Nisha, D Devi Sumangala

Citation Information : N, Sumangala DD. A Case of Mucopolysaccharidosis II /I-Cell Disease. J South Asian Feder Obs Gynae 2013; 5 (1):45-46.

DOI: 10.5005/jp-journals-10006-1220

Published Online: 01-08-2015

Copyright Statement:  Copyright © 2013; The Author(s).


Abstract

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  1. Clinical diagnosis of lysosomal storage diseases. In: Applegarth DA, Dimmick JE, Hall JG (Eds). Organelle diseases: Clinical features, diagnosis, pathogenesis and management. Londons: Chapman and Hall 1997;37-71.
  2. Prevalence of lysosomal storage disorders. JAMA 1999;281:249-54.
  3. I-cell disease (mucolipidosis type II). http://www.emedicine.com/ped/topic1150.htm. Updated December 12, 2003. Accessed July 2004.
  4. The osteodystrophy of mucolipidosis type III and the effects of intravenous pamidronate treatment. J Inherit Metab Dis 2002;25:681-93.
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