ASXL-Related Disorders Natural History Study
Recruiting
Observational Study
Bohring-Opitz Syndrome
ASXL1 Gene Mutation
Shashi-Pena Syndrome
ASXL2 Gene Mutation
Bainbridge-Ropers Syndrome
ASXL3 Gene Mutation
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Sex
- Any
- Study type
- Observational
- Participants needed
- 200 (estimated)
- Sponsor
- University of California, Los Angeles · Other
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About This Trial
A registry focused on the natural history, management and treatment of patients with Bohring-Opitz Syndrome (ASXL1), Shashi-Pena Syndrome (ASXL2) and Bainbridge-Ropers Syndrome (ASXL3).
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Clinical or molecular diagnosis of an ASXL related disorder
Exclusion Criteria:
* No clinical or molecular diagnosis of an ASXL related disorder
Contacts