Occipital cortex dysgenesis with white matter changes due to mutations in Laminin a2

Laminin α2 related congenital muscular dystrophy is one of the most common congenital muscular dystrophies of childhood with or without clinical evidence of central nervous system involvement. It may be associated with significant white matter abnormalities resembling leukodystrophies. In this stud...

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Bibliographic Details

Published in:	The Turkish Journal of Pediatrics
Main Authors:	Uluç Yiş, Vishal Dixit, Sedat Işıkay, Mert Karakaya, Figen Baydan, Gülden Diniz, İpek Polat, Semra Hız-Kurul, Sebahattin Çırak
Format:	Article
Language:	English
Published:	Hacettepe University Institute of Child Health 2017-06-01
Subjects:	congenital muscular dystrophy dysgenesis laminin α2 occipital cortex
Online Access:	https://turkjpediatr.org/article/view/997