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    1,308 Possible Causes for Li Fraumeni Syndrome in USA

    • Leukemia
      Li-Fraumeni Syndrome

      Also, children who have inherited certain genetic problems — such as Li-Fraumeni syndrome, Down syndrome , Klinefelter syndrome , neurofibromatosis , ataxia telangectasia,[] Children with certain genetic conditions, such as Down syndrome or Li-Fraumeni syndrome, are at increased risk of developing leukemia.[]

    • Malignant Neoplasm of the Breast
      Li-Fraumeni Syndrome

      Prognosis Complications Li-Fraumeni Syndrome [57] This includes those who carry the BRCA1 and BRCA2 gene mutation . [57] These mutations account for up to 90% of the total[] As far as the etiology is concerned, Li-Fraumeni syndrome (germline TP53 mutation) has been reported to increase the risk of phyllodes tumors ( 3 , 4 ).[] Li-Fraumeni syndrome: Characterized by early onset breast cancers, sarcomas, brain tumours, adrenal cortical tumours and acute leukemias.[]

    • Malignant Melanoma
      Li-Fraumeni Syndrome
    • Li-Fraumeni Syndrome

      "Li-Fraumeni Syndrome".[] "Correction: a Li-Fraumeni syndrome p53 mutation.[] "Germline TP53 mutations and Li-Fraumeni syndrome".[]

    • Li-Fraumeni Syndrome 1

      Li-Fraumeni syndrome type 1 (TP53) DNA Test Deatils about the test Li-Fraumeni syndrome type 1 (TP53) What is the cost of Li-Fraumeni syndrome type 1 (TP53) ?[] […] a appointment time for Li-Fraumeni syndrome type 1 (TP53) Free home collection for Li-Fraumeni syndrome type 1 (TP53) Receive reports online for Li-Fraumeni syndrome type[] Billing for Li-Fraumeni syndrome type 1 (TP53) 100% money back guaranty for Li-Fraumeni syndrome type 1 (TP53)[]

    • Ruijs Aalfs Syndrome

      AB - Background Li-Fraumeni syndrome (LFS) is a rare autosomal dominant cancer predisposition syndrome.[] syndrome: mutation detection rate and relative frequency of cancers in different familial phenotypes", abstract "Background Li-Fraumeni syndrome (LFS) is a rare autosomal[] PY - 2010/6 Y1 - 2010/6 N2 - Background Li-Fraumeni syndrome (LFS) is a rare autosomal dominant cancer predisposition syndrome.[]

    • Ayerza Syndrome

      In a study, it was observed that 50% of Li-Fraumeni syndrome family members developed a second sarcoma in the radiotherapy field [ 5 ].[] Discussion Li-Fraumeni syndrome is a rare cancer predisposition disorder that is associated with germline mutations of the p53 tumor suppressor gene.[] Clinical diagnosis of classic Li-Fraumeni syndrome is a proband with sarcoma diagnosed before age 45, a first degree relative with any cancer before age 45, and a first or[]

    • Eng-Strom Syndrome

      The Li-Fraumeni syndrome.[] Prenatal diagnosis in Li-Fraumeni syndrome.[] Germline TP53 mutations and Li-Fraumeni syndrome.[]

    • Familial Hyperlipidemia

      Li-Fraumeni syndrome in aMalaysian kindred.[] The first documentationof Li-Fraumeni syndrome in Korea.[] Mutations of germ-cell line TP53 gene are mainly reported in LiFraumeni syndrome(LFS).[]

    • Choroid Plexus Tumor

      This young patient developed a rhabdomyosarcoma, which strongly suggests Li-Fraumeni syndrome.[] ETIOLOGY/PATHOGENESIS Sporadic Tumors Most choroid plexus tumors are sporadic, but choroid plexus carcinomas are strongly associated with germline TP53 mutations Li-Fraumeni[] Syndrome Tumor predisposition syndrome most commonly secondary to germline TP53 mutations Most CNS neoplasms in Li-Fraumeni patients are astrocytomas ( 60%) Also develop[]

    Further symptoms

    Similar symptoms