Literature DB >> 14652450

X-linked lissencephaly in an Indian family.

S Panda1, M Tripathi, S Jain, P Sharma.   

Abstract

Neuronal migration disorders are an important differential diagnosis to be considered in the evaluation of intractable epilepsy. Though the underlying causative factors which govern their development are many and varied, genetic factors have been found to be contributory in a few forms of these disorders. An X-linked association with lissencephaly has recently been discovered and there are a few families described till now with this entity.

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Year:  2003        PMID: 14652450

Source DB:  PubMed          Journal:  Neurol India        ISSN: 0028-3886            Impact factor:   2.117


  1 in total

1.  Autosomal recessive type I lissencephaly.

Authors:  Ajay Garg; M R Sridhar; Sheffali Gulati
Journal:  Indian J Pediatr       Date:  2007-02       Impact factor: 1.967

  1 in total

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