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Li-Fraumeni syndrome

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Clinical Trials

This information is provided by ClinicalTrials.gov

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Displaying 1-5 of 5 results.
Screening With Whole Body MRI For Detection Of Primary Tumors In Children And Adults With Li-Fraumeni Syndrome (LFS) And Other Cancer Predisposition Syndromes
Status: Recruiting
Last Changed: Feb 05, 2020
First Received: Nov 01, 2016
Disease(s): Li-Fraumeni Syndrome
Intervention(s): Whole Body MRI
Locations: Dana Farber Cancer Institute, Boston, Massachusetts, United States
Memorial Sloan-Kettering Cancer Center, New York, New York, United States
Li-Fraumeni Syndrome/TP53 Biobank
Status: Recruiting
Last Changed: May 01, 2020
First Received: Apr 29, 2020
Disease(s): Li-Fraumeni Syndrome, Li-Fraumeni-Like Syndrome
Intervention(s): No Intervention
Locations: Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States
University of Pennsylvania, Philadelphia, Pennsylvania, United States
Clinical and Genetic Studies of Li-Fraumeni Syndrome
Status: Recruiting
Last Changed: May 07, 2020
First Received: Sep 29, 2011
Disease(s): Li-Fraumeni Syndrome, Neoplasms, Tp53 Mutations
Locations: National Institutes of Health Clinical Center, 9000 Rockville Pike, Bethesda, Maryland, United States
Characterization of Patients With Uncommon Presentations and/or Uncommon Diseases Associated With the Cardiovascular System
Status: Recruiting
Last Changed: Jun 16, 2020
First Received: Jun 14, 2010
Disease(s): Cardiomyopathy, Li-Fraumeni Syndrome, Parkinson's Disease, Atherosclerosis, Cardiovascular Capacity
Locations: National Institutes of Health Clinical Center, 9000 Rockville Pike, Bethesda, Maryland, United States
Familial Investigations of Childhood Cancer Predisposition
Status: Recruiting
Last Changed: May 08, 2020
First Received: Feb 10, 2017
Disease(s): 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
Locations: St. Jude Children's Research Hospital, Memphis, Tennessee, United States