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Saul-Wilson Syndrome clinical trials

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NCT ID: NCT04569149 Recruiting - Clinical trials for Meier-Gorlin Syndrome

Primordial Dwarfism Registry

Start date: March 11, 2008
Phase:
Study type: Observational [Patient Registry]

The goal of this registry is to collect information on individuals with Microcephalic Osteodysplastic Primordial Dwarfism Type II (also called MOPDII) and other forms of microcephalic primordial dwarfism. The study team hopes to learn more about these conditions and improve the care of people with it by establishing this registry.