Clinical, genetic and neuropathological findings in a series of 138 fetuses with a corpus callosum malformation

CONCLUSIONIn our series of 138 cases of CCM, prenatal and postmortem examinations identified a variety of genetic causes. However, no diagnosis could be established in 67% of cases. The classification based on the underlying neurodevelopmental defects paves the way for further genetic studies and genotype‐phenotype correlations. Birth Defects Research (Part A), 2015. © 2015 Wiley Periodicals, Inc.

Source: Birth Defects Research Part A: Clinical and Molecular Teratology - December 14, 2015 Category: Perinatology & Neonatology Authors: Caroline Alby, Valérie Malan, Lucile Boutaud, Maria Angela Marangoni, Bettina Bessières, Maryse Bonniere, Amale Ichkou, Nadia Elkhartoufi, Nadia Bahi‐Buisson, Pascale Sonigo, Anne‐Elodie Millischer, Sophie Thomas, Yves Ville, Michel Vekemans, Férec Tags: Obituary Source Type: research