Clinical trial
GROWing Up With Rare GENEtic Syndromes ….When Children With Complex Genetic Syndromes Reach Adult Age
NCT04463316 is registered in ClinicalTrials.gov with dr. Laura C. G. de Graaff-Herder as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- GROWing Up With Rare GENEtic Syndromes ….When Children With Complex Genetic Syndromes Reach Adult Age
- Lead sponsor
- dr. Laura C. G. de Graaff-Herder
- Phase
- Observational
- Overall status
- Recruiting
- Start date
- October 1, 2018
- Completion date
- January 1, 2030
- Enrollment
- 600 (estimated)
- Sites
- 1
Conditions
As the registry lists them; a condition with its own page is linked.
17p- deletiesyndrome, 1q25-32 deletie, 22q11 deletion syndrome, 46, xy dsd, albright hereditaire osteodystrofie, allan-herndon-dudley syndrome, bardet biedl syndrome, charge syndrome, congenital adrenal hyperplasia, congenital hypopituitarism, cornelia de lange syndrome, disorders of sex development, jacobsen syndrome / 11 q syndrome, kallmann syndrome, klinefelter (xxy-)syndrome, myrhe syndrome, neurofibromatosis, noonan syndrome, ohdo syndrome, polr3a mutatie, prader-willi syndrome, pws-like syndrome, rare bone disorders, rett syndrome, saethre-chotzen syndrome, silver russel syndrome, tuberous sclerosis, turner syndrome, vcf syndrome, williams-beuren syndrome, xxxx syndrome (tetra-x syndrome), xxxxy syndrome, xxyy syndrome