Is Celiac Disease Genetic?

The question of whether celiac disease is genetic is a very curious question. People with celiac disease are wondering why they have encountered this disease. For this reason, celiac studies the answer to the question of genetics. In this article, we will answer the question of whether celiac disease is genetic.

Is Celiac Genetic?

Almost all people with celiac disease carry a type of gene for the disease that can also be passed on to their children. If your mother, father, or anyone with whom you are a first-degree relative has celiac disease, there is a high probability that you will also have celiac disease. Celiac disease is a genetic disease.

There are two types of genes carried for celiac disease. These genes are medically referred to as human leukocyte antigen (HLA) DQ2 and DQ8. Many people with celiac disease may have both of these genes or have at least one. In very rare cases, although a person does not have these genes, celiac disease can still occur.

Celiac disease is a genetically highly related condition, and if one person has celiac disease in families, it also occurs in other people with blood ties. However, having a relative with a celiac disease condition (even a first-degree relative such as a child, brother, sister, or parent) does not guarantee that you will develop this condition. In some cases, celiac disease is not observed in the child, even if it is in the family.

If you or your partner want to find out if your child will have celiac disease, you can have a genetic test.

Celiac Disease in Children

Celiac disease in children; it can usually occur genetically. If the parents have celiac disease, there is a very high probability that the child may also have celiac disease. If either of the spouses has celiac disease and you have child planning or have a small child, it is possible to find out if your child will have this disease thanks to genetic tests.

Celiac Disease in Children is Genetic

Celiac disease in children Genetic tests can help you find out if your child will develop celiac disease in the future. If you or your partner carry a gene for celiac disease, celiac disease can also be passed on to your children. However, carrying a gene does not mean that your child will definitely have celiac disease. It means that your child is at risk of developing celiac disease.

The specialist doctor you applied for celiac disease genetic testing can detect this condition thanks to a blood test. A positive HLA DQ2 or DQ8 value in the test results indicates that your child is at risk for developing celiac disease. This indicator definitely does not mean that they will get celiac disease or that their chances of getting celiac disease are already low. But you should have blood tests at regular December intervals to see if your child has blood markers, in other words blood signs, for celiac disease.

On the contrary, if the celiac disease genetic test results were negative for HLA DQ2 or DQ8 values, your child does not carry the celiac disease genes. In negative cases, it is not possible to develop, develop celiac disease, or for parents to pass this disease on to their children. Sometimes it can be difficult for doctors to read the test results. You should talk to a doctor who understands the genetics of celiac disease and knows a lot about celiac disease. If you choose to have your child genetically tested for celiac disease, the doctor may review the results.

Celiac disease genetic tests are very important. You can find out whether you or your child may be at risk of celiac disease through these tests. People are at risk of developing celiac disease at any point in their lives. You can find out if you carry the celiac disease genes that may be passed on to your children in the future.

Who Should Have a Celiac Disease Genetic Test?

If you are thinking about who should have a genetic test for celiac disease; our answer is in this part. Those who follow a gluten-free diet, celiac patients, and anyone with a relative who has celiac disease should undergo genetic testing to find out if their child will have celiac disease in the future.

People who are currently following a gluten-free diet should also undergo genetic testing, even if they are following a gluten-free diet. Following a gluten-free diet relieves the symptoms of celiac disease; it does not cure the disease.

People who have not had a small bowel biopsy but have been on a gluten-free diet for a long time should also have this test. A positive genetic test will increase the likelihood that the symptoms that lead to a gluten-free diet are caused by celiac disease, but it will not confirm the diagnosis. The only way to confirm the diagnosis of celiac disease is to stop the diet and then have a small bowel biopsy. In addition, a test with a negative result does not exclude the diagnosis of the disease: this means that October diagnosis is unlikely, but not impossible. In this case, it is recommended to consider other diagnoses.

If any of your relatives have celiac disease, you should definitely get a genetic test. In cases of first-degree kinship, the probability is very high. If you receive a diagnosis of celiac disease at an early stage, you will not be late for your treatment before serious symptoms occur.