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PMID: 16969376 Published · ppublish English Journal Article

Sotos syndrome.

European journal of human genetics : EJHG ·Vol. 15 ·No. 3 ·2007-03-00 ·Pages 264-71

Tatton-Brown K, Rahman N

Abstract

Sotos syndrome is an autosomal dominant condition characterised by a distinctive facial appearance, learning disability and overgrowth resulting in tall stature and macrocephaly. In 2002, Sotos syndrome was shown to be caused by mutations and deletions of NSD1, which encodes a histone methyltransferase implicated in chromatin regulation. More recently, the NSD1 mutational spectrum has been defined, the phenotype of Sotos syndrome clarified and diagnostic and management guidelines developed.

MeSH Terms
Body Height/genetics Facies Histone Methyltransferases Histone-Lysine N-Methyltransferase Humans Intracellular Signaling Peptides and Proteins/genetics Learning Disabilities/genetics,pathology Nuclear Proteins/genetics Skull/abnormalities Syndrome
Chemicals
Intracellular Signaling Peptides and Proteins Nuclear Proteins Histone Methyltransferases Histone-Lysine N-Methyltransferase NSD1 protein, human
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Tatton-Brown Katrina
Section of Cancer Genetics, Institute of Cancer Research, Sutton, Surrey, UK.
Rahman Nazneen
Article Info
Journal
European journal of human genetics : EJHG
Abbr.
Eur J Hum Genet
ISSN
1018-4813
Published
2007-03-00
Epub
2006-00-13
Pages
264-71
Language
English
Region
England
NLM ID
9302235
Subset
IM
Grants
Medical Research Council · G0400188 · United Kingdom
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