Literature DB >> 25329715

Neuropsychological profiles of patients with 2q37.3 deletion associated with developmental dyspraxia.

Kaeko Ogura1, Kenzo Takeshita, Chikako Arakawa, Keiko Shimojima, Toshiyuki Yamamoto.   

Abstract

Patients with 2q37 deletions manifest brachydactyly mental retardation syndrome (BDMR). Recent advances in human molecular research have revealed that alterations in the histone deacetylase 4 gene (HDAC4) are responsible for the clinical manifestations of BDMR. Here, we report two male patients with 2q37.3 deletions. One of the patients showed a typical BDMR phenotype, and HDAC4 was included in the deletion region. HDAC4 was preserved in the other patient, and he showed a normal intelligence level with the delayed learning of complex motor skills. Detailed neuropsychological examinations revealed similar neuropsychological profiles in these two patients (visuo-spatial dyspraxia) that suggested developmental dyspraxia. These observations suggested that some other candidate genes for neuronal development exist in the telomeric region of HDAC4.
© 2014 Wiley Periodicals, Inc.

Entities:  

Keywords:  2q37.3 deletion; Albright hereditary osteodystrophy-like syndrome (AHO-like); autism spectrum disorder; brachydactyly mental retardation syndrome (BDMR); developmental dyspraxia; histone deacetylase 4 gene (HDAC4); intellectual disability

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Year:  2014        PMID: 25329715     DOI: 10.1002/ajmg.b.32274

Source DB:  PubMed          Journal:  Am J Med Genet B Neuropsychiatr Genet        ISSN: 1552-4841            Impact factor:   3.568


  2 in total

1.  Brief psychotic episode in a patient with chromosome 2q37 microdeletion syndrome.

Authors:  Kevin Lally; Nuraini Ibrahim; Mary Kelly; Gautam Gulati
Journal:  BMJ Case Rep       Date:  2017-11-27

2.  Characterization of two familial cases presenting with a syndromic specific learning disorder and carrying (17q;21q) unbalanced translocations.

Authors:  Julie Coton; Audrey Labalme; Marianne Till; Gerald Bussy; Sonia Krifi Papoz; Gaetan Lesca; Delphine Heron; Damien Sanlaville; Patrick Edery; Vincent des Portes; Massimiliano Rossi
Journal:  Clin Case Rep       Date:  2018-03-09
  2 in total

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