Literature DB >> 3960322

Miller-Dieker syndrome: a disorder affecting specific pathways of neuronal migration.

L A Alvarez, T Yamamoto, B Wong, T J Resnick, J F Llena, S L Moshé.   

Abstract

A patient with the typical craniofacial features and clinical course of Miller-Dieker syndrome (MDS) was found on autopsy to have focal pachygyria rather than lissencephaly. The brainstem and cerebellum were hypoplastic, but thalami and basal ganglia were normal. We believe that MDS is a syndrome in which multiple specific pathways of neuronal migration are affected selectively, such as migration to the neocortex, migration via corpus pontobulbare, and cerebellar migration. However, another migration pathway (via corpus gangliothalamicum) is spared.

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Year:  1986        PMID: 3960322     DOI: 10.1212/wnl.36.4.489

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  3 in total

1.  Heterotopic gray matter. Report of a case.

Authors:  A Arena; D Scuderi
Journal:  Ital J Neurol Sci       Date:  1990-06

2.  Clinical and molecular diagnosis of Miller-Dieker syndrome.

Authors:  W B Dobyns; C J Curry; H E Hoyme; L Turlington; D H Ledbetter
Journal:  Am J Hum Genet       Date:  1991-03       Impact factor: 11.025

3.  INTERNEURONOPATHIES AND THEIR ROLE IN EARLY LIFE EPILEPSIES AND NEURODEVELOPMENTAL DISORDERS.

Authors:  Anna-Maria Katsarou; Solomon L Moshé; Aristea S Galanopoulou
Journal:  Epilepsia Open       Date:  2017-06-28
  3 in total

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