Families living with Noonan Syndrome say there is a pressing need for more social support and awareness of the rare genetic condition. Loughborough University researchers have spoken with more than 60 ...

Vosoritide's first global Phase II study showed an average increased growth rate of 1.8 cm per year in children with hypochondroplasia, a genetic cause of short stature in children, according to ...

Patients with clinical features suggestive of either NS, NSML, CFC, NF1, Legius syndrome or Noonan-like syndrome; patients with a clinical diagnosis of any of these syndromes that previously tested ...