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Sjogren Larsson Syndrome in three siblings of an Indian family
Author(s) -
Akanksha Gupta,
Gunjan Mishra,
Anubha Jain,
Chandra Kanta
Publication year - 2014
Publication title -
journal of pediatric sciences
Language(s) - English
Resource type - Journals
ISSN - 1309-1247
DOI - 10.17334/jps.15884
Subject(s) - medicine , psychology , dermatology
Sjogren Larsson Syndrome (SLS) is an uncommon autosomal recessive disorder characterized by intellectual disability, congenital icthyosis and spastic diplegia. Here we report three siblings with SLS  from an Indian family with no history of consanguinity. One sibling had unusual features of spasticity and tremors in upper limbs.

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