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Primordial Dwarfism Registry

Recruitingn/aAges any - anyAllNemours Children's Clinic
NCT04569149 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

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.

Sign in to get the eligibility rules as simple questions to take to your doctor.

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📋 Eligibility rules (as published)
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 a medical provider, are eligible for this registry. Exclusion Criteria: * individuals without microcephalic primordial dwarfism or closely related conditions
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What it tests

  • Not listed
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Where

1 site
Nemours
Wilmington, United States
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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