| Literature DB >> 25329715 |
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.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