CenterWatch
  • Search Clinical Trials
  • Clinical Trial Listings
  • Volunteer
  • Learn About Clinical Trials

Wolf Hirschhorn Syndrome

Wolf-Hirschhorn Syndrome is a rare genetic disorder that is caused by a deletion on the short arm of chromosome 4. It is characterized by distinctive facial features, intellectual disability, delayed growth and development, and seizures. The severity of symptoms can vary widely, even among individuals with the same genetic mutation.

Entire World
Filters

Type

Distance
Age
0
0
Gender
Trial Phase
Sponsor
CenterWatch

5000 Centregreen Way, Suite 200
Cary, NC, 27513, USA

Phone: 703.538.7600
Toll Free: 888.838.5578

  • Disclaimer
  • Privacy Policy
  • Term of Use
  • Do Not Sell My Personal Information