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

> **NCT03139903** · — · COMPLETED · sponsor: **Assistance Publique - Hôpitaux de Paris** · enrollment: 30 (actual)

## Conditions studied

- Microcephalic Osteodysplastic Primordial Dwarfism Type II
- Seckel Syndrome

## Interventions

_None listed._

## Key facts

- **NCT ID:** NCT03139903
- **Lead sponsor:** Assistance Publique - Hôpitaux de Paris
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** COMPLETED
- **Start date:** 2010-07-28
- **Primary completion:** 2013-07-16
- **Final completion:** 2015-07
- **Target enrollment:** 30 (ACTUAL)
- **Last updated:** 2017-11-20


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT03139903

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT03139903, "The Primordial Dwarfisms: Diagnosis, Identification of the Molecular Basis of Seckel Syndrome and Microcephalic Osteodysplastic Primordial Dwarfism Type II". Retrieved via AI Analytics 2026-05-27 from https://api.ai-analytics.org/clinical/NCT03139903. Licensed CC0.

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