IDMet (RaDiCo Cohort) (RaDiCo-IDMet)
Recruiting
Observational Study
Silver Russell Syndrome
Beckwith-Wiedemann Syndrome
Transient Neonatal Diabetes Mellitus
Angelman Syndrome
Prader-Willi Syndrome
Temple Syndrome
Kagami-Ogata Syndrome
Pseudohypoparathyroidism
Familial Precocious Puberty
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Sex
- Any
- Study type
- Observational
- Participants needed
- 2,000 (estimated)
- Sponsor
- Institut National de la Santé Et de la Recherche Médicale, France · Government
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About This Trial
The goal of this observational study is to describe the natural history of imprinting disorders (IDs) according to their metabolic profile in all patients (adults and children) affected with an ID regardless of the severity of the disease, with a molecular characterization, with a signed informed consent for all subjects, followed in one partner's center.
The main questions it aims to answer are:…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Patients (adults and children) affected with an ID regardless of the severity of the disease
* A confirmed diagnosis of ID (based on molecular diagnosis)
* A signed informed consent for adults or signed informed consent of parents/guardians of minors/ protected adult.
Non-Inc…
Contacts