Clinical Trials

27 trials
RecentStart dateEnrollment
OTHER × Observational × Tuberous Sclerosis × Clear all
NCT03050268 2026-04-23

SJFAMILY

St. Jude Children's Research Hospital

Recruiting
1,500 enrolled
BreastCNSClassical hematologyDermatologicEndocrineGastrointestinalGynecologicLymphoidOther solid neoplasmSarcoma

Turcot syndrome, Juvenile polyposis syndrome, Choroid Plexus Carcinoma, GATA2 Deficiency, Basal Cell Nevus Syndrome, Colorectal Neoplasms, Hereditary Nonpolyposis, Fanconi Anemia, Hamartoma Syndrome, Multiple, von Hippel-Lindau Disease, Hodgkin Disease, Lymphoma, Non-Hodgkin, Melanoma, Neuroblastoma, Neurofibromatosis 1, Noonan Syndrome, Pancreatic Neoplasms, Paraganglioma, Peutz-Jeghers Syndrome, Pheochromocytoma, Rothmund-Thomson Syndrome, Adenomatous Polyposis Coli, Retinoblastoma, Rhabdomyosarcoma, Tuberous Sclerosis, Neurofibromatosis 2, Li-Fraumeni Syndrome, Adrenocortical Carcinoma, Multiple Endocrine Neoplasia Type 1, Multiple Endocrine Neoplasia Type 2a, Dyskeratosis Congenita, Genetic Predisposition to Disease, Anemia, Diamond-Blackfan, Carney Complex, Hereditary Breast and Ovarian Cancer Syndrome

NCT06523582 2024-07-26

Genetic Bases of Neuroendocrine Neoplasms in Mexican Patients

Universidad Nacional Autonoma de Mexico

Recruiting
750 enrolled
CNSEndocrineGastrointestinalHead & NeckNETSarcoma

Carney-Stratakis Syndrome, Carney Triad, Pituitary Adenoma, Familial Isolated, Colorectal Neoplasms, Hereditary Nonpolyposis, Hamartoma Syndrome, Multiple, von Hippel-Lindau Disease, Adenoma, Islet Cell, Neurofibromatosis 1, Paraganglioma, Pheochromocytoma, Pituitary Neoplasms, Tuberous Sclerosis, Li-Fraumeni Syndrome, Carcinoma, Medullary, Neuroendocrine Tumors, Multiple Endocrine Neoplasia Type 1, Multiple Endocrine Neoplasia Type 2a, Gastrointestinal Stromal Tumors, Hyperparathyroidism, Primary, Carney Complex

NCT06065852 2023-10-04

RaDaR

UK Kidney Association

Recruiting
35,000 enrolled
Classical hematologyGenitourinaryPlasma cell

Renal cysts and diabetes syndrome, Hypomagnesemia primary, Nephronophthisis, familial juvenile, Renal tubular acidosis, distal, autosomal recessive, Adenine phosphoribosyltransferase deficiency, SeSAME syndrome, Hematuria, Benign Familial, Hypophosphatemic Rickets with Hypercalciuria, Hereditary, Nephrogenic Syndrome of Inappropriate Antidiuresis, Hypomagnesemia 1, Intestinal, Immunoglobulin Light-chain Amyloidosis, Fabry Disease, Bartter Syndrome, Calciphylaxis, Cystinosis, Cystinuria, Fibromuscular Dysplasia, Glomerulonephritis, IGA, Glomerulosclerosis, Focal Segmental, Glycosuria, Renal, Hyperoxaluria, Primary, Nail-Patella Syndrome, Nephritis, Hereditary, Nephrosis, Lipoid, Nephrotic Syndrome, Oculocerebrorenal Syndrome, Pseudohypoaldosteronism, Red-Cell Aplasia, Pure, Retroperitoneal Fibrosis, Tuberous Sclerosis, Vasculitis, Glomerulonephritis, Membranoproliferative, Glomerulonephritis, Membranous, Polycystic Kidney, Autosomal Dominant, Polycystic Kidney, Autosomal Recessive, Diabetes Insipidus, Nephrogenic, Denys-Drash Syndrome, Gitelman Syndrome, Liddle Syndrome, Dent Disease, Atypical Hemolytic Uremic Syndrome

NCT04463316 2023-09-06

GROW UR GENES

Erasmus Medical Center

Recruiting
600 enrolled
CNS

Blepharophimosis syndrome Ohdo type, Tetrasomy X, Allan-Herndon-Dudley syndrome, Acrocephalosyndactylia, Adrenal Hyperplasia, Congenital, De Lange Syndrome, DiGeorge Syndrome, Klinefelter Syndrome, Noonan Syndrome, Prader-Willi Syndrome, Disorders of Sex Development, Tuberous Sclerosis, Turner Syndrome, Rett Syndrome, Neurofibromatoses, Kallmann Syndrome, Williams Syndrome, Bardet-Biedl Syndrome, Jacobsen Distal 11q Deletion Syndrome, 22q11 Deletion Syndrome, Disorder of Sex Development, 46,XY, CHARGE Syndrome