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help you understand whether an inherited health condition may affect you, your child or another family member, and help you decide whether to have children show if you are at higher risk of getting certain health conditions, including some types of cancer
If you or a family member has a serious genetic condition, you may be worried about one or more of your children inheriting that condition. In these cases, you have several options available to...
How cystic fibrosis is inherited. To be born with cystic fibrosis, a child has to inherit a copy of the faulty gene from both of their parents. This can happen if the parents are "carriers" of the faulty gene, which means they don't have cystic fibrosis themselves.
Navigating daily life when affected by a genetic, rare or undiagnosed condition can be challenging. As well as the need to manage medical appointments, you might encounter hurdles in areas of your life such as education and work, childcare and family planning, finances and social situations.
If you think that your child may have a genetic condition, talk to your GP or SENCO at school about your concerns. They will be able to explain the appropriate route for further referrals. Back to top. How your child might be affected. Genetic conditions can vary widely according to which genes are affected.
Jul 2, 2024 · If you’re diagnosed with an inherited heart condition, your first-degree family members (parents, siblings and children) should be assessed for the same condition. Symptoms of inherited heart conditions. An inherited heart condition can cause symptoms like: dizzy spells; blackouts, faints or fits (seizures) palpitations; breathlessness; chest ...
If your child has symptoms of an inherited condition or one that might be caused by a spontaneous gene mutation, your doctor may recommend genetic testing.
