Analysis of the NSD1 promoter region in patients with a Sotos syndrome phenotype

Remco Visser, Tomonobu Hasegawa, Norio Niikawa, Naomichi Matsumoto

研究成果: Article査読

3 被引用数 (Scopus)

抄録

Sotos syndrome (SoS, OMIM#117550) is an overgrowth disorder characterized by excessive growth - especially in the first years of childhood - distinctive craniofacial features, and various degrees of mental retardation. Haploinsufficiency of the nuclear receptor binding SET domain containing protein 1 (NSD1) gene, due to either intragenic mutations or whole-gene microdeletions, is found in the majority of patients with SoS. However, in approximately 10-40% of patients with a typical SoS phenotype, no abnormalities are detected. In this study, hemizygous hypermethylation or genomic sequence abnormalities of the promoter region of NSD1 were hypothesized to be the underlying cause in patients with a SoS phenotype, but without confirmed NSD1 alterations. In 18 patients, including one patient with a reported hepatocellular carcinoma, the promoter region of NSD1 was analyzed. However, no hypermethylation or sequence abnormalities in the promoter region could be detected. It therefore seems unlikely that such abnormalities of NSD1 are a major culprit in patients with phenotypical SoS. Additional methods are necessary for detection of other genetic or epigenetic causes of SoS.

本文言語English
ページ(範囲)15-20
ページ数6
ジャーナルJournal of Human Genetics
51
1
DOI
出版ステータスPublished - 2006 1月

ASJC Scopus subject areas

  • 遺伝学
  • 遺伝学(臨床)

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