Some people have inherited gene faults that increase their risk of developing particular types of cancer. Some gene faults can increase the risk of more than one type of cancer. If a close member of your family has had one or more of the types of cancer mentioned below you may like to read the relevant information. Bowel cancer is the 4th most common type of cancer in the UK.
Some inherited genes can increase the risk of developing bowel cancer and cause the conditions mentioned here.
A faulty APC gene can cause hundreds of non cancerous benign growths called polyps to are all cancers genetic in the bowel at a young age. If left untreated, all people with this syndrome will almost certainly develop bowel cancer by their 40s. Some people can develop FAP without any history of bowel cancer in their family.
This means that the gene fault has happened for the first time in that person. It is much rarer than FAP familial adenomatous polyposis. People with MAP develop polyps and are likely to develop bowel cancer under the age of Most of the bowel cancers occur under the age of People with Lynch syndrome also have an increased risk of developing other cancers including womb and ovarian cancer in women.
Other cancers that Lynch syndrome may cause include stomach, small bowel and gallbladder. These are all rare and most people with Lynch syndrome do not develop these other cancers. If someone has PJS, the skin around the mouth, nostrils, are all cancers genetic, eyes, and near the back passage may be darker than surrounding skin. PJS is very rare are all cancers genetic it is difficult to find any reliable figures about how many bowel cancers it may cause.
A fault in one of these genes can cause polyps in the stomach and small bowel. Juvenile is the name of the type of polyp and is not related to the age at which the polyps develop. It is not clear how much JPS increases the risk of developing bowel cancer.
If a close member of your family has had bowel or womb cancer and you are worried that you may be at higher risk, see your GP. Your GP can check your family history and refer you to a genetic clinic if necessary. If you have one of the inherited bowel conditions or you are known to have a gene fault that increases bowel cancer risk, your specialist are all cancers genetic suggest that you have regular bowel screening. Find out about screening for people at high risk of bowel cancer, are all cancers genetic.
Breast cancer is a common cancer and 1 in 8 women develop it during their lifetime in the UK. Occasionally when someone who benzoyl alcohol lotion had breast cancer has a test for the BRCA genes the test can show changes in another gene such as CHEK2, but much less is known about most of the other genes. These genes also increase the risk of ovarian cancer and BRCA2 increases the risk of male breast cancer and prostate cancer.
The TP53 gene normally controls when a cell divides. It is a type of tumour suppressor gene. It causes breast cancer as part of a rare cancer syndrome called Li Fraumeni syndrome.
PTEN is the gene fault that causes a rare condition called Cowden syndrome. It increases the risk of breast cancer. They are known to increase breast cancer risk.
It is unclear if the risk of ovarian cancer is increased. Women can have one or more of these gene changes, are all cancers genetic. Finding these changes has helped scientists understand how breast cancer are all cancers genetic. It might be several years before tests are developed for these other genes. If a close member of are all cancers genetic family has had breast or ovarian cancer and you are worried that you may be at higher risk, see your GP.
Read about breast cancer genes and gene testing. If you are known to have a gene that increases your breast cancer risk, your specialist will suggest that you have regular screening or treatments to reduce your risk. Depending on your age and how high your risk is you may consider having risk reducing breast surgery.
Read about screening and treatment for women at higher risk of breast cancer. Kidney cancer is the are all cancers genetic most common cancer in the UK. We know that if a person has a family history of kidney cancer their risk is increased. This may be because of a shared way 3m advanced allergy filter life or more rarely because of inherited faulty genes, are all cancers genetic.
Researchers are looking aluminum can airplane plans which genes may increase the risk of developing kidney cancer.
We know that there are a number of inherited conditions that increase the risk of developing it. They include the conditions below.
Kidney cysts are common in VHL syndrome. These cysts do not usually affect how the kidney works, but sometimes a type of kidney cancer called clear cell renal cell cancer CCRCC can develop in a cyst, are all cancers genetic.
People who carry the gene fault also have an increased risk of developing other rare cancers in the brain, spine, pancreas, eyes and inner ear.
It can cause skin, brain and heart problems, as well as kidney disease. People with TS have an increased risk of kidney cysts and papillary kidney cancer. People with BHDS develop multiple benign skin tumours fibrofolliculomas on the face, neck and upper body. People with BHDS are at increased risk of kidney cancer. It is a very rare condition and the number of people and families with BHDS is not known.
Doctors may suspect it in families when several family members have papillary renal cell carcinoma. People with HLRCC have benign skin tumours cutaneous leiomyomatafibroids in the womb uterine leiomyomataand may have kidney cancer, are all cancers genetic.
Papillary renal cancer is the most common kidney cancer type in HLRCC, but other types, such as tubulo papillary renal cell cancer and collecting duct renal cell cancer, can develop. If a close member of your family has had kidney cancer and you are worried that you may be at higher risk, see your GP.
Read about testing for cancer risk genes, are all cancers genetic. Melanoma is a type of cancer that usually occurs in the skin. In the UK, around 15, people are diagnosed with melanoma each year.
The main cause of melanoma is too much exposure to ultraviolet light, from sunlight or from artificial sources such as sun beds. People with a family history of melanoma are at increased risk.
Researchers have found that familial atypical multiple mole melanoma syndrome FAMMM increases the risk of developing melanoma. People who have FAMMM have more than 50 moles and at least one close relative has been diagnosed with a melanoma. A close relative is a parent, brother, are all cancers genetic, sister, child, aunt, uncle or grandparent.
Research suggests that the risk of melanoma linked to the CDKN2A fault varies depending on where in the world someone lives. For example, people who live in Australia have a higher risk than those in the UK. If close members of your family have had melanoma and you are worried that you may be at higher risk, see your GP. Read about screening for people at higher risk of melanoma. Lynch syndrome is more commonly linked to bowel cancer but can also increase the are all cancers genetic of ovarian cancer.
If close members of your family have had ovarian, breast or bowel cancer at a young age and you are worried that you may be at higher risk, see your GP. If you have a faulty gene that increases the risk of ovarian cancer, what happens next will depend on which gene you have, are all cancers genetic. Your specialist may suggest regular screening. Researchers are looking into the best way to do this.
Read about screening and treatment for women at high risk of ovarian cancer. Cancer of the pancreas can also develop as part of one of the family cancer syndromes, when different types of cancer occur in the same family. The genes mentioned here can increase the risk of other types of cancer as well as pancreatic cancer.
If close members of your family have had pancreatic cancer and you are worried that you may be at higher risk, see your GP. Researchers are looking into the best way are all cancers genetic monitoring people with a strong family history of pancreatic cancer. If your doctor thinks you have a strong family history, you may be able to have regular screening as part of a research project.
Read about screening for people at higher risk of pancreatic cancer. Prostate cancer is now the most common cancer in men. It is most common over the age of Scientists have found a number of genes that increase the risk of prostate cancer. At the moment there is only a test available for the BRCA2 gene, are all cancers genetic. This gene is more commonly linked to breast and ovarian cancer. We need more research to find out whether it does increase the risk.
If close members of your family have had prostate cancer and you are worried that you may be at higher risk, see your GP. If you have a gene test and a faulty gene is found, what happens next depends on which gene is faulty. Read about screening for men at higher risk of prostate cancer. Retinoblastoma is a rare cancer that develops in young children. Around 45 children get retinoblastoma every year in the UK. Most cases occur are all cancers genetic the age of 5 years.
Children who have a parent, or brother or sister, who had retinoblastoma should be checked for retinoblastoma. They usually have screening from birth to the age of 3 years. This involves regular eye examinations under a general anaesthetic.