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The Official Scientific Journal of Delhi Ophthalmological Society
Inclusion Cell Disease - A Rare Cause of Megalocornea with Corneal Edema
Namrata1, Rahul Ranjan2, Gaurav Arya3 
1Department of Ophthalmology, Sadguru Netra Chikitsalaya, Madhya Pradesh, India
2Department of Radio-Diagnosis, Rama Medical College, Kanpur, Uttar Pradesh,India
3Department of Paediatrics, Rama Medical College, Kanpur, Uttar Pradesh, India
Corresponding Author:
Rahul Ranjan 
MD, DNB
Associate Professor, 
Rama Medical College, 
Mandhana, Kanpur, Uttar Pradesh, India
Email id: rahulranjanradio10@gmail.com
Published Online: 30-APR-2018
DOI: http://dx.doi.org/10.7869/djo.354
Abstract
Inclusion cell disease (I cell disease), also known as mucolipidosis type II, is a rare congenital metabolic storage disorder which seemingly occupies an intermediate position between mucopolysaccharidosis and sphingolipidosis.1 We are hereby presenting a case of I cell disease that presented with megalocornea and corneal edema/corneal clouding. 
Keywords : Inclusion cell disease, mucolipidosis, sphingolipidosis, megalocornea, corneal edema, corneal clouding.
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