Turcot Syndrome
National Organization for Rare Disorders, Inc.
Synonyms ...
Turcot Syndrome
What is Turcot syndrome?
Turcot syndrome is one of several conditions in which cells become abnormal and form one or more masses called polyps. Polyps are benign (noncancerous) but can eventually turn cancerous.
Turcot Syndrome: Turcot's syndrome is characterized by the concurrence of a primary malignant brain tumor and multiple colorectal adenomas. Patients are also at risk for developing multiple basal cell cancers of the scalp, and stomach cancer.
Turcot syndrome.
In most cases, the cause of CNS embryonal tumors is not known.
The symptoms of childhood CNS embryonal tumors are not the same in every child.
Gardner Syndrome
Turcot Syndrome
familial adenomatous polyposis
attenuated FAP ...
These disorders include Turcot syndrome, Peutz-Jeghers syndrome, juvenile polyposis coli, and MYH-associated polyposis.
Genetics and Cancer--Familial Adenomatous Polyposis (FAP) ...
Turcot syndrome (brain tumors and colonic polyposis)
Familial adenomatous polyposis an inherited mutation of the APC gene that leads to early onset of colon carcinoma.
These include Turcot syndrome, an inherited condition in which people are at an increased risk of adenomatous polyps (and thus, colon cancer) and brain tumors, and Peutz-Jeghers syndrome, ...
abnormalities that are associated with CNS neoplasms) include neurofibromatosis type I (17q11), neurofibromatosis type II (22q12), von Hippel-Lindau disease (3p25-26), tuberous sclerosis (9q34, 16p13), Li-Fraumeni syndrome (17p13), Turcot syndrome ...
For example, people with the hereditary diseases called neurofibromatosis type 1, Turcot syndrome, Li-Fraumeni cancer syndrome, and tuberous sclerosis have a higher than average risk of developing a glioma.
Von Recklinghausen disease, also called neurofibromatosis 1 (NF1 gene) and neurofibromatosis 2 (NF2 gene)
Turcot syndrome (APC gene)
Gorlin syndrome, also called basal cell nevus syndrome (PTCH gene)
Tuberous sclerosis (TSC1 and TSC2 genes) ...
Certain inherited conditions, including neurofibromatosis, Von Hippel-Lindau syndrome, Li-Fraumeni syndrome, and Turcot syndrome
Personal history of cancer or family history of brain cancer
Impaired immune system ...
Neurofibromatosis type 1 or 2
von Hippel-Lindau disease
Tuberous sclerosis
Li-Fraumeni syndrome
Turcot syndrome type 1 and type 2
Klinefelter syndrome
Nevoid basal cell carcinoma syndrome ...
Some individuals may have a genetic predisposition to colorectal cancer associated with the genes for familial adenomatous polyposis (Gardner syndrome, Turcot syndrome) and hereditary nonpolyposis syndromes.
HNPCC is also known as the Lynch syndrome after Dr. Henry Lynch at Creighton University in Omaha, Nebraska. HNPCC includes the Muir-Torre Syndrome and Turcot Syndrome.
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Turcot Syndrome
Turner Phenotype with Normal Chromosomes (Karyotype)
Turner Syndrome
Turner Syndrome Society of Canada - Support Group
Turner Syndrome Society of Canada - Turner's Syndrome - Support Group
Turner Syndrome Society of the U.S.
Some inherited conditions increase the risk of brain tumors, including neurofibromatosis, Von Hippel-Lindau syndrome, Li-Fraumeni syndrome, and Turcot syndrome.
Association of Multiple Polyps of the Colon and a Primary Tumour of the Central Nervous System see Turcot syndrome
Asthma
Asymmetry Dwarfism see Silver-Russell syndrome
Ataxia-telangiectasia ...
There doesn't appear to be a genetic predisposition, meaning the disease does not seem to run in families. Certain conditions have an increased association with PNETs. These include: Li-Fraumeni syndrome, Turcot syndrome and Gorlin syndrome.
cell phones, cordless phones, and wireless devices are safe and do not increase the risk.
Some inherited conditions increase the risk of brain tumors, including neurofibromatosis, Von Hippel-Lindau syndrome, Li-Fraumeni syndrome, and Turcot syndrome.
 See also: Cancer, Symptom, Brain tumor, Surgery, Radiation therapy
  
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