GROWing Up With Rare GENEtic Syndromes
Recruiting
Observational Study
Prader-Willi Syndrome
PWS-like Syndrome
Silver Russel Syndrome
Congenital Hypopituitarism
Klinefelter (XXY-)Syndrome
Congenital Adrenal Hyperplasia
XXXXY Syndrome
XXYY Syndrome
XXXX Syndrome (Tetra-X Syndrome)
Disorders of Sex Development
Turner Syndrome
46, XY DSD
Tuberous Sclerosis
Neurofibromatosis
Albright Hereditaire Osteodystrofie
Cornelia de Lange Syndrome
Saethre-Chotzen Syndrome
17p- Deletiesyndrome
VCF Syndrome
POLR3A Mutatie
Ohdo Syndrome
Jacobsen Syndrome / 11 q Syndrome
Myrhe Syndrome
CHARGE Syndrome
1q25-32 Deletie
Bardet Biedl Syndrome
Rett Syndrome
22q11 Deletion Syndrome
Allan-Herndon-Dudley Syndrome
Kallmann Syndrome
Rare Bone Disorders
Noonan Syndrome
Williams-Beuren Syndrome
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Observational
- Participants needed
- 600 (estimated)
- Sponsor
- dr. Laura C. G. de Graaff-Herder · Other
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About This Trial
Introduction Rare complex syndromes Patients with complex genetic syndromes, by definition, have combined medical problems affecting multiple organ systems, and intellectual disability is often part of the syndrome. During childhood, patients with rare genetic syndromes receive multidisciplinary and specialized medical care; they usually receive medical care from 3-4 medical specialists.
Increase…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Patients with rare syndromes or rare congenital diseases visiting the multidisciplinary outpatient clinic for patients with rare diseases at the department of endocrinology, internal medicine, Erasmus Medical Center.
Exclusion Criteria:
* None
Contacts
No contact information available.