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Clinical geneticist for children

20 April 2022

What is a clinical geneticist?

A clinical geneticist is a doctor who specializes in diagnosing and treating people with genetic conditions. Clinical geneticists use their knowledge of genetics to help identify the cause of a person’s symptoms and make recommendations for treatment.

What do clinical geneticists do?

Clinical geneticists work with patients and families to determine if a genetic condition is the cause of a person’s symptoms. If a genetic condition is suspected, clinical geneticists may order tests to confirm the diagnosis. Once a diagnosis is made, clinical geneticists work with patients and families to develop a treatment plan.

Why would you see a clinical geneticist?

If you or your child has symptoms that may be caused by a genetic condition, your doctor may refer you to a clinical geneticist. You may also see a clinical geneticist if you have a family history of a genetic condition.

There are many different genetic conditions that clinical geneticists can diagnose. Some of the more common conditions include Down syndrome, cystic fibrosis, and sickle cell disease.

What to expect when you see a clinical geneticist?

When you see a clinical geneticist for the first time, they will take a detailed medical history. They will also ask about your family history. Be prepared to answer questions about your symptoms and any medical problems that run in your family. The clinical geneticist may also order tests, such as blood tests or genetic tests. These tests can help confirm a diagnosis of a genetic condition.

After taking your medical history and ordering tests, the clinical geneticist will review the results and make a diagnosis. If a genetic condition is diagnosed, the clinical geneticist will work with you to develop a treatment plan. The treatment plan may include medication, surgery, or lifestyle changes.

If you or your child has symptoms that may be caused by a genetic condition, it is important to see a clinical geneticist. Clinical geneticists are experts in diagnosing and treating genetic conditions. They will work with you to develop a treatment plan that is right for you or your child.

If you think you or your child may benefit from seeing a clinical geneticist, talk to your doctor.

What to do before going to a clinical geneticist?

If you have been referred to a clinical geneticist, there are a few things you can do to prepare for your appointment.

First, make a list of all of your child’s symptoms. Be sure to include when the symptoms started and how often they occur.

Next, gather information about your family history. This may include medical conditions that run in your family, as well as the names and contact information for family members who have been diagnosed with a genetic condition.

Finally, write down any questions you want to ask the clinical geneticist. This may include questions about your child’s diagnosis, treatment options, or how to cope with a diagnosis of a genetic condition.

By preparing for your appointment, you can make sure that you get the most out of your visit with the clinical geneticist.

When should I see a clinical geneticist?

You may benefit from seeing a clinical geneticist if you or your child has symptoms that may be caused by a genetic condition. Clinical geneticists are experts in diagnosing and treating genetic conditions.

You may also benefit from seeing a clinical geneticist if you have a family history of a genetic condition. Clinical geneticists can order tests to check for conditions that run in families. They can also provide information about how to reduce the risk of passing on a genetic condition to your children.

What therapies are available for children with genetic conditions?

The type of therapy that is best for a child with a genetic condition will depend on the specific condition. Some common treatments include medication, surgery, and lifestyle changes.

Medication: Medication can be used to treat many different genetic conditions. For example, medication can be used to control seizures in children with epilepsy.

Surgery: Surgery may be needed to treat some genetic conditions. For example, surgery can be used to correct a heart defect in a child with congenital heart disease.

Lifestyle changes: Lifestyle changes may be needed to treat some genetic conditions. For example, children with sickle cell disease may need to take steps to avoid dehydration.

The best treatment for a child with a genetic condition will be determined by the child’s doctor. Treatment options will vary depending on the specific condition.

It is important to remember that there is no one-size-fits-all approach to treating children with genetic conditions. The best treatment plan will be tailored to the individual child and their specific needs.

If you have a child with a genetic condition, talk to your doctor about the best treatment options for your child.

What support is available in Australia for children with genetic conditions?

If your child has been diagnosed with a genetic condition, there are many support services available in Australia.

Your local health department can provide information about support groups and services in your area.

The Australian Genetic Support Network (AGSN) is a national organisation that provides support and information to people affected by genetic conditions. The AGSN can be contacted on 1800 260 3601 or by visiting their website at agsn.org.au.

The Genetic Counsellors Society of Australia (GCSA) is another national organisation that provides support and information to people affected by genetic conditions. The GCSA can be contacted on 1300 363 4867 or by visiting their website at gcsa.org.au.

If your child has been diagnosed with a genetic condition, there are many support services available in Australia. These organisations can provide you with information and support to help you cope with your child’s diagnosis.

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