Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
3036755 | Brain and Development | 2016 | 4 Pages |
Abstract
Mutations in the ARFGEF2 gene must be considered in the presence of bilateral periventricular nodular heterotopia and putaminal hyperintensity in children presenting with movement disorder, severe developmental delay and microcephaly. In case of ARFGEF2 gene mutation, screening for cardiomyopathy may be indicated.
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Authors
Sanem Yilmaz, Sarenur Gokben, Gul Serdaroglu, Cenk Eraslan, Grazia M.S. Mancini, Hande Tekin, Hasan Tekgul,