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- W2138045587 abstract "We report three related and one unrelated child with an apparently novel neurodevelopmental disorder. The clinical course was very similar in all the four patients: congenital microcephaly with severe failure of post-natal brain growth, neonatal onset of intractable seizures associated with lack of developmental progression and death within the first 3 years of life. The appearance on cerebral neuroimaging was almost identical, with simplified gyration associated with a non-thickened cortex, severe hypoplasia of the corpus callosum, a small flattened brain stem, and specific cystic lesions in the white matter around the temporal and occipital horns. To our knowledge these patients represent a previously unreported, autosomal recessive syndrome. Homozygosity mapping in the consanguineous family has identified a candidate region on the chromosome 2p16." @default.
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- W2138045587 date "2005-11-04" @default.
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- W2138045587 title "Leucodysplasia, microcephaly, cerebral malformation (LMC): a novel recessive disorder linked to 2p16" @default.
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- W2138045587 doi "https://doi.org/10.1093/brain/awh663" @default.
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