Literature DB >> 16188863

Auxological data in patients clinically suspected of Sotos syndrome with NSD1 gene alterations.

Lonneke de Boer1, Saskia le Cessie, Jan M Wit.   

Abstract

AIM: Nuclear receptor-binding SET domain-containing protein 1 (NSD1) gene mutations and deletions (NSD1+/-) are the major cause of Sotos syndrome. The aim was to investigate which auxology parameters relate to NSD1+/- in patients clinically suspected of Sotos syndrome.
METHODS: In 32 patients clinically suspected of Sotos syndrome, we compared auxology parameters between NSD1+/- patients and patients without NSD1 gene alterations (NSD1+/+). The statistical performance of these parameters to predict NSD1+/- was assessed.
RESULTS: Arm span-for-height standard deviation score (SDS) and hand length SDS were significantly higher in NSD1+/- patients.
CONCLUSION: Arm span for height and hand length are discriminating parameters between NSD1+/- and NSD1+/+.

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Year:  2005        PMID: 16188863     DOI: 10.1111/j.1651-2227.2005.tb02059.x

Source DB:  PubMed          Journal:  Acta Paediatr        ISSN: 0803-5253            Impact factor:   2.299


  1 in total

1.  Sotos syndrome with a novel mutation in the NSD1 gene associated with congenital hypothyroidism.

Authors:  Arushi Verma; Parisa Salehi; Anne Hing; Alissa Jeanne Curda Roberts
Journal:  Int J Pediatr Adolesc Med       Date:  2020-06-26
  1 in total

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