Clinical Trials on Noonan Syndrome

Total 16 results





    • NCT04463316
      Recruiting
      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; 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 Syndrome
    • NCT04395495
      Recruiting
      Conditions: RAS Mutation; Neurofibromatosis 1; Noonan Syndrome; Noonan Syndrome With Multiple Lentigines; Noonan Neurofibromatosis Syndrome; Cardiofaciocutaneous Syndrome; Costello Syndrome; Legius Syndrome; Smith-Kingsmore Syndrome; MTOR Gene Mutation; GATOR-1 Gene Mutation; SYNGAP1-Related Intellectual Disability; DLG4; MAPK1 Gene Mutation
    • NCT04219007
      Recruiting
      Conditions: Short Stature
    • NCT03504501
      Recruiting
      Conditions: Impaired Synaptic Plasticity; Impaired Cognition
    • NCT03435627
      Active, not recruiting
      Conditions: Genetic Disorder; Noonan Syndrome
    • NCT03050268
      Recruiting
      Conditions: Acute Leukemia; Adenomatous Polyposis; Adrenocortical Carcinoma; AML; BAP1 Tumor Predisposition Syndrome; Carney Complex; Choroid Plexus Carcinoma; Constitutional Mismatch Repair Deficiency Syndrome; Diamond-Blackfan Anemia; DICER1 Syndrome; Dyskeratosis Congenita; Emberger Syndrome; Familial Acute Myeloid Leukemia; Familial Adenomatous Polyposis; Fanconi Anemia; Familial Cancer; Familial Wilms Tumor; Familial Neuroblastoma; GIST; Hereditary Breast and Ovarian Cancer; Hereditary Paraganglioma-Pheochromocytoma Syndrome; Hodgkin Lymphoma; Juvenile Polyposis; Li-Fraumeni Syndrome; Lynch Syndrome; MDS; Melanoma Syndrome; Multiple Endocrine Neoplasia Type 1; Multiple Endocrine Neoplasia Type 2; Neuroblastoma; Neurofibromatosis Type 1; Neurofibromatosis Type II; Nevoid Basal Cell Carcinoma Syndrome; Non Hodgkin Lymphoma; Noonan Syndrome and Other Rasopathy; Overgrowth Syndromes; Pancreatic Cancer; Peutz-Jeghers Syndrome; Pheochromocytoma/Paraganglioma; PTEN Hamartoma Tumor Syndrome; Retinoblastoma; Rhabdoid Tumor Predisposition Syndrome; Rhabdomyosarcoma; Rothmund-Thomson Syndrome; Tuberous Sclerosis; Von Hippel-Lindau Disease
    • NCT02713945
      Recruiting
      Conditions: Noonan Syndrome
    • NCT02486731
      Unknown status
      Conditions: Noonan Syndrome; LEOPARD Syndrome
    • NCT02383316
      Completed
      Conditions: Child Syndrome
    • NCT01927861
      Completed
      Conditions: Genetic Disorder; Noonan Syndrome
    • NCT01556568
      Withdrawn
      Conditions: Cardiomegaly
    • NCT01529840
      Completed
      Conditions: Genetic Disorder; Noonan Syndrome
    • NCT01529944
      Completed
      Conditions: Genetic Disorder; Noonan Syndrome
    • NCT00960128
      Completed
      Conditions: Growth Hormone Disorder; Growth Hormone Deficiency in Children; Adult Growth Hormone Deficiency; Genetic Disorder; Turner Syndrome; Foetal Growth Problem; Small for Gestational Age; Chronic Kidney Disease; Chronic Renal Insufficiency; Noonan Syndrome
    • NCT00452725
      Completed
      Conditions: Noonan Syndrome
    • NCT00351221
      Terminated
      Conditions: Noonan Syndrome