Incidence of cCPHD in Denmark – a National Observational Study
Condition(s):Combined Pituitary Hormone Deficiency Genetic Form; Combined Pituitary Hormone DeficiencyLast Updated:July 7, 2022Active, not recruiting
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Condition(s):Combined Pituitary Hormone Deficiency Genetic Form; Combined Pituitary Hormone DeficiencyLast Updated:July 7, 2022Active, not recruiting
Condition(s):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 SyndromeLast Updated:September 6, 2023Recruiting
Condition(s):Congenital or Acquired HypopituitarismLast Updated:June 3, 2022Not yet recruiting
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