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Neuropsychological profiles of patients with 2q37.3 deletion associated with developmental dyspraxia
Author(s) -
Ogura Kaeko,
Takeshita Kenzo,
Arakawa Chikako,
Shimojima Keiko,
Yamamoto Toshiyuki
Publication year - 2014
Publication title -
american journal of medical genetics part b: neuropsychiatric genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.393
H-Index - 126
eISSN - 1552-485X
pISSN - 1552-4841
DOI - 10.1002/ajmg.b.32274
Subject(s) - hdac4 , neuropsychology , phenotype , psychology , genetics , neuroscience , audiology , medicine , gene , biology , cognition , histone , histone deacetylase
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.