Primordial Dwarfism Registry
Recruiting
Observational Study
MOPDII
Meier-Gorlin Syndrome
Saul-Wilson Syndrome
Microcephalic Primordial Dwarfism
IMAGe Syndrome
RNU4atac-opathy (e.g MOPDI, Lowry-Wood Syndrome, and Roifman Syndrome)
LIG4 Syndrome
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
- Nemours Children's Clinic · Other
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About This Trial
The goal of this registry is to collect information on individuals with forms of microcephalic primordial dwarfism as well as related conditions. The study team hopes to learn more about these conditions and improve the care of people with them by establishing this registry.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Individuals with MOPDII, Meier-Gorlin syndrome, IMAGe syndrome, RNU4atac-opathies (MOPDI/III, Roifman syndrome, Lowry-Wood syndrome), LIG4 syndrome, and other classified as well as unclassified types of microcephalic primordial dwarfism and related conditions, as diagnosed by …
Contacts