GROWing Up With Rare GENEtic Syndromes

Conditions:   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;   T urner 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 Intervention:   Diagnostic Test: Retrospective file studies Sponsor:   dr. Laura C. G. de Graaff-Herder Recruiting
Source: ClinicalTrials.gov - Category: Research Source Type: clinical trials