Login / Signup

The Clinical Cases of Geleophysic Dysplasia: One Gene, Different Phenotypes.

Evgenia GlobaNataliya ZelinskaAndrew Dauber
Published in: Case reports in endocrinology (2018)
Patients with severe dwarfism, skeletal anomalies, and other specific syndromic features (e.g., tracheal stenosis and cardiac valvulopathy) should undergo genetic testing to exclude acromelic dysplasia syndromes.
Keyphrases
  • left ventricular
  • genome wide
  • copy number
  • early onset
  • gene expression
  • dna methylation
  • drug induced
  • autism spectrum disorder
  • transcription factor