We do not know exactly what causes Parkinson’s disease (PD), but scientists believe that a combination of genetic and environmental factors is the cause. The extent to which each factor is involved varies from person to person. Researchers do not know why some people develop Parkinson’s and others do not.

Genetics causes about 10% to 15% of all Parkinson’s. In some families, changes (or mutations) in certain genes are inherited or passed down from generation to generation. A handful of ethnic groups, like the Ashkenazi Jews and North African Arab Berbers, more commonly carry genes linked to PD and researchers are still trying to understand why.

A genetic test will help you identify whether you carry a genetic mutation related to Parkinson’s. Understanding genetic differences across people with Parkinson’s can help identify clues about how and why a person’s experience with the disease differs from others. Genetic tests are not a substitute for a Parkinson’s diagnosis.

We are here for you.

Dr. Chayim Schell-Apacik is a specialist in clinical genetics with over three decades of experience in supporting patients. We offer individualised evaluations, genetic consultation, and testing, with the goal to providing you with genetic information that presents choices and minimises uncertainty, empowering you to make decisions that are most beneficial for you. Please contact us, to find out more.

What is genetic testing?

Genetic testing – sometimes called genomic testing, finds changes in the genetic material that can cause health problems. It is mainly used to diagnose rare and inherited health conditions and some cancers.
You may be offered a genetic test because your doctor thinks

• you or your child might have a health condition caused by a change in the genetic material involving one or more genes or certain chromosomes.
• someone in your family has a health condition that is caused by changes in the genetic material involving one or more genes, or certain chromosomes.
• some of your close relatives have had a particular type of cancer that could be inherited.

At Schell Genetics, we are here to assist you in this process. Please don’t hesitate to contact us.

Learn more about other RARE DISEASES or GENETIC DISORDERS