Literature DB >> 2290486

Ataxia, developmental delay and an extensive neuronal migration abnormality in 2 siblings.

M G Harbord1, S Boyd, M A Hall-Craggs, B Kendall, M A McShane, M Baraitser.   

Abstract

Two siblings with developmental delay and a non-progressive cerebellar ataxia are described. The electroencephalograms in both children showed a rather unusual pattern of high amplitude 10-12/s rhythms maximal anteriorly, while extensive neuronal migration abnormalities were apparent on Magnetic Resonance scans. There were no dysmorphic features, metabolic abnormalities, chromosomal defects or evidence of prenatal environmental toxins. It is considered that these siblings have an autosomal recessive neuronal migration defect which has not previously been reported.

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Year:  1990        PMID: 2290486     DOI: 10.1055/s-2008-1071501

Source DB:  PubMed          Journal:  Neuropediatrics        ISSN: 0174-304X            Impact factor:   1.947


  6 in total

Review 1.  Genetics of the polymicrogyria syndromes.

Authors:  A Jansen; E Andermann
Journal:  J Med Genet       Date:  2005-05       Impact factor: 6.318

2.  Three Mutations in the Bilateral Frontoparietal Polymicrogyria Gene GPR56 in Pakistani Intellectual Disability Families.

Authors:  Humaira Aziz Sawal; Ricardo Harripaul; Anna Mikhailov; Kayla Vleuten; Farooq Naeem; Tanveer Nasr; Muhammad Jawad Hassan; John B Vincent; Muhammad Ayub; Muhammad Arshad Rafiq
Journal:  J Pediatr Genet       Date:  2017-12-21

3.  GPR56-regulated granule cell adhesion is essential for rostral cerebellar development.

Authors:  Samir Koirala; Zhaohui Jin; Xianhua Piao; Gabriel Corfas
Journal:  J Neurosci       Date:  2009-06-10       Impact factor: 6.167

Review 4.  GPR56 and the developing cerebral cortex: cells, matrix, and neuronal migration.

Authors:  Kathleen Singer; Rong Luo; Sung-Jin Jeong; Xianhua Piao
Journal:  Mol Neurobiol       Date:  2012-09-22       Impact factor: 5.590

5.  Subcortical laminar heterotopia and lissencephaly in two families: a single X linked dominant gene.

Authors:  J M Pinard; J Motte; C Chiron; R Brian; E Andermann; O Dulac
Journal:  J Neurol Neurosurg Psychiatry       Date:  1994-08       Impact factor: 10.154

6.  G-protein coupled receptor 56 promotes myoblast fusion through serum response factor- and nuclear factor of activated T-cell-mediated signalling but is not essential for muscle development in vivo.

Authors:  Melissa P Wu; Jamie R Doyle; Brenda Barry; Ariane Beauvais; Anete Rozkalne; Xianhua Piao; Michael W Lawlor; Alan S Kopin; Christopher A Walsh; Emanuela Gussoni
Journal:  FEBS J       Date:  2013-10-08       Impact factor: 5.542

  6 in total

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