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GROWing Up With Rare GENEtic Syndromes

GROWing Up With Rare GENEtic Syndromes

Recruiting
18 years and older
All
Phase N/A
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Study details
    Prader-Willi Syndrome
    Noonan Syndrome
    Male Pseudohermaphroditism
    Tuberous Sclerosis
    Neurofibromatosis
    Neurofibromatosis
    Hermaphroditism
    Rett Syndrome
    Cornelia De Lange Syndrome
    Kallmann's Syndrome
    CHARGE Syndrome
    CONNECTIVE TISSUE DISEASE
    dermatomyositis (connective tissue disease)
    Congenital adrenal hyperplasia
    Congenital adrenal hyperplasia
    Hypogonadism
    Hypogonadism
    Klinefelter's Syndrome
    Congenital Heart Defect
    Congenital Heart Disease
    NF1 gene
    Williams Syndrome
    Hereditary Neoplastic Syndrome
    hereditary cancer syndromes
    Bardet-Biedl Syndrome
    Obesity
    Obesity
    DiGeorge Syndrome
    Turner's Syndrome
    Saethre-Chotzen Syndrome
    22q11 Deletion Syndrome
    Congenital Heart Disease
    dermatomyositis (connective tissue disease)
    hereditary cancer syndromes
    PWS-like Syndrome
    Silver Russel Syndrome
    Congenital Hypopituitarism
    XXXX Syndrome (Tetra-X Syndrome)
    Albright Hereditaire Osteodystrofie
    17p- Deletiesyndrome
    POLR3A Mutatie
    Ohdo Syndrome
    Jacobsen Syndrome / 11 q Syndrome
    Myrhe Syndrome
    1q25-32 Deletie
    Allan-Herndon-Dudley Syndrome
    Rare Bone Disorders

NCT04463316

dr. Laura C. G. de Graaff-Herder

19 February 2024

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