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- W1996510080 abstract "Pachygyria is a disorder of neuronal migration. We report an Indian family with four siblings with developmental delay, infrequent seizures, normal head size and mild to moderate mental retardation. Two of them had bilaterally symmetrical frontotemporal pachygyria. Dysmorphism and neurological signs were absent in the affected subjects. Affected male and female siblings with normal parents suggests autosomal recessive mode of inheritance. We believe these cases represent a new autosomal recessive disorder of neuronal migration. Other similar cases of lissencephaly are reviewed." @default.
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- W1996510080 date "2007-01-01" @default.
- W1996510080 modified "2023-09-23" @default.
- W1996510080 title "A new autosomal recessive disorder of bilateral frontotemporal pachygyria without microcephaly: Report of a case and review of literature" @default.
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- W1996510080 doi "https://doi.org/10.4103/0028-3886.30429" @default.
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