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Seckel Syndrome clinical trials

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NCT ID: NCT03139903 Completed - Seckel Syndrome Clinical Trials

The Primordial Dwarfisms: Diagnosis, Identification of the Molecular Basis of Seckel Syndrome and Microcephalic Osteodysplastic Primordial Dwarfism Type II

NANPIM
Start date: July 28, 2010
Phase: N/A
Study type: Observational

The purpose of this study si to define morphological and epidemiological parameters and identify new symptoms in French patients with Seckel syndrome (SCKL) or microcephalic osteodysplastic primordial dwarfism type II (MOPDII).