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Track this trial| NCT Number | NCT04463316 |
| Lead Sponsor | dr. Laura C. G. de Graaff-Herder |
| Conditions (from sponsor) |
Prader-Willi Syndrome, PWS-like Syndrome, Silver Russel Syndrome, Congenital Hypopituitarism, Klinefelter (XXY-)Syndrome, Congenital Adrenal Hyperplasia, XXXXY Syndrome, XXYY Syndrome +25 more |
| Related terms | 22q11 Deletion Syndrome, Acrocephalosyndactylia, Adrenal Hyperplasia, Congenital, Allan-Herndon-Dudley syndrome, Bardet-Biedl Syndrome, Blepharophimosis syndrome Ohdo type, CHARGE Syndrome, De Lange Syndrome, DiGeorge Syndrome, Disorder of Sex Development, 46,XY, Disorders of Sex Development, Jacobsen Distal 11q Deletion Syndrome, Kallmann Syndrome, Klinefelter Syndrome, Neurofibromatoses, Noonan Syndrome, Prader-Willi Syndrome, Rett Syndrome, Tetrasomy X, Tuberous Sclerosis, Turner Syndrome, Williams Syndrome |
| Enrollment | 600 participants |
| Start Date | |
| Primary Completion | (estimated) |
| Study Completion | (estimated) |
| Updated on ClinicalTrials.gov |