References in periodicals archive
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In addition to those genetic mutations, an increased risk of endometrial cancer is found among women with hereditary nonpolyposis colon cancer (Lynch syndrome).
Lindor, "Familial colorectal cancer type X: the other half of hereditary nonpolyposis colon cancer syndrome," Surgical Oncology Clinics of North America, vol.
Mutations of two PMS homologues in hereditary nonpolyposis colon cancer. Nature, 371: 75-80.
Mecklin, "Genotype and phenotype in hereditary nonpolyposis colon cancer: a study of families with different vs.
Also, if you have a family history or have been diagnosed with hereditary nonpolyposis colon cancer (HNPCC), you should be screened for uterine cancer every year beginning at age 35.
Populations at increased risk of developing ovarian cancer include women with BRCA1 and BRCA2 genetic mutations, Lynch syndrome (hereditary nonpolyposis colon cancer), or a family history of ovarian cancer.
Mutation screening in the hMLH1 gene in Swedish hereditary nonpolyposis colon cancer families.
Hereditary nonpolyposis colon cancer is caused by a defect in certain genes.
* If your family has a history of colorectal and related cancers, you may want to consider genetic testing for mutations in two genes strongly associated with hereditary nonpolyposis colon cancer (HNPCC).
Patients who had familial adenomatous polyposis or hereditary nonpolyposis colon cancer, inflammatory bowel diseases, or previous colon surgery were excluded.
* Hereditary nonpolyposis colon cancer. Genetic testing can be done by screening for mutations in the MSH2 or MLH1 mismatch repair gene or by searching a patient's tumor for microsatellite instability.
As in genetic testing for hereditary nonpolyposis colon cancer (HNPCC), an affected family member should first be tested.
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- hereditary elliptocytosis
- hereditary folate malabsorption
- hereditary fructose intolerance
- hereditary haemorrhagic telangiectasia
- hereditary hearing impairment
- hereditary hemochromatosis
- hereditary hemorrhagic telangiectasia
- hereditary hypersegmentation of neutrophils
- hereditary hyperthyroidism
- hereditary hypophosphatemic rickets
- hereditary lymphedema
- hereditary lymphoedema
- hereditary metaphyseal dysostosis
- hereditary mixed polyposis syndrome
- hereditary motor & sensory neuropathy
- hereditary motor sensory neuropathy
- hereditary multiple exostoses
- hereditary mutation
- hereditary myokymia
- hereditary myopathy with early respiratory failure
- hereditary neoplasia
- hereditary nephritis
- hereditary nephritis and nerve deafness
- hereditary neuralgic amyotrophy
- hereditary neuropathy with pressure palsies
- hereditary nonpolyposis colon cancer
- hereditary nonpolyposis colorectal cancer
- hereditary non-polyposis colorectal cancer type 3
- hereditary opalescent dentin
- hereditary orotic aciduria
- hereditary persistence of fetal hemoglobin
- hereditary photomyoclonus
- hereditary preneoplasia
- hereditary progressive arthroophthalmopathy
- hereditary proteinuria syndromes
- hereditary pseudohaemophilia
- hereditary pyropoikilocytosis
- hereditary renal hypouricuria
- hereditary sensory and autonomic neuropathy
- hereditary sensory and autonomic neuropathy type 2A
- hereditary sensory and autonomic neuropathy type 6
- hereditary sensory neuropathy
- hereditary sensory radicular neuropathy
- hereditary spastic paraplegia
- hereditary spherocytosis
- hereditary spinal ataxia
- hereditary thrombophilia
- hereditary tyrosinaemia
- hereditary xerocytosis
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- hereditary nephritis
- hereditary nephritis and nerve deafness
- Hereditary Nephritis Foundation
- Hereditary Neuralgic Amyotrophy
- Hereditary Neuralgic Amyotrophy
- Hereditary Neurological Disease Centre
- hereditary neuronal abiotrophy of Swedish Lapland dogs
- hereditary neuronal abiotrophy of Swedish Lapland dogs
- hereditary neuronal abiotrophy of Swedish Lapland dogs
- hereditary neuronal abiotrophy of Swedish Lapland dogs
- hereditary neuropathy
- hereditary neuropathy
- hereditary neuropathy
- hereditary neuropathy
- Hereditary Neuropathy with Liability to Pressure Palsies
- Hereditary Neuropathy with Liability to Pressure Palsies
- Hereditary Neuropathy with Pressure Palsies
- Hereditary Neuropathy with Pressure Palsies
- hereditary neutropenia
- hereditary non-haemolytic bilirubinaemia
- hereditary non-haemolytic cholaemia
- hereditary non-haemolytic jaundice
- Hereditary non-polyposis colon cancer
- Hereditary non-polyposis colon cancer
- Hereditary Non-Polyposis Colon Cancer Syndrome
- Hereditary Non-Polyposis Colorectal
- hereditary non-polyposis colorectal cancer type 3
- Hereditary Non-Polypotic Colorectal Cancer
- Hereditary non-spherocytic hemolytic anemia
- Hereditary non-spherocytic hemolytic anemia
- hereditary nonpolyposis colon cancer
- Hereditary nonpolyposis colorectal cancer
- Hereditary Nonpolyposis Colorectal Cancer Syndrome Carcinomas
- Hereditary Nonpolyposis Colorectal Cancer Type 4
- Hereditary Nonpolyposis Colorectal Cancer/Carcinoma
- Hereditary Nonspherocytic Hemolytic Anemia
- hereditary oligophrenic cerebellolental degeneration
- hereditary oligophreniccerebellolental degeneration
- Hereditary Onycho-Osteodysplasia
- hereditary opalescent dentin
- hereditary opalescent dentin
- hereditary opalescent dentin
- hereditary opalescent teeth
- hereditary opalescent teeth
- hereditary optic neuritis
- hereditary optic neuritis
- hereditary optic neuritis
- hereditary optic neuropathy
- hereditary optic neuropathy
- hereditary optic neuropathy
- Hereditary optic neuroretinopathy
- hereditary orotic aciduria
- Hereditary Palmo-Plantar Keratoderma
- Hereditary pancreatitis
- Hereditary Papillary Renal Cell Carcinoma
- Hereditary Papulotranslucent Acrokeratoderma
- hereditary pattern
- Hereditary Periodic Fever Syndrome
- Hereditary Persistence of Alpha-Fetoprotein
- Hereditary Persistence of Fetal Hemoglobin
- Hereditary Persistence of Fetal Hemoglobin
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