

If you’ve ever asked yourself, “Is Parkinson’s genetic?” or “Will I pass it on to my kids?” — you’re not alone. These are some of the most common and emotionally loaded questions we hear at The Center for Movement Challenges. Whether you’ve just been diagnosed or have a family member with Parkinson’s disease, understanding the role of genetics can bring clarity, relief, and a sense of control.
Let’s look at what the science actually says.
Parkinson’s is a neurodegenerative disorder that affects movement and is caused by a gradual loss of dopamine-producing brain cells. The root cause can vary from person to person and is typically influenced by a mix of genetic and environmental factors.
In most cases, Parkinson’s is considered idiopathic, which means the exact cause is unknown. However, that doesn’t mean genes don’t play a role.
The short answer: sometimes.
Genetics are thought to play a role in about 10 to 15 percent of Parkinson’s cases. These are considered familial Parkinson’s disease cases, where the condition runs in families and is tied to identifiable genetic mutations.
Scientists have identified several genes linked to Parkinson’s, including:
Mutations in these genes can increase the risk of developing Parkinson’s, especially in families where multiple members are affected.
Not always. There’s a difference between something being genetic and being hereditary.
While some forms of Parkinson’s are hereditary, the vast majority are not. Even if a person carries a Parkinson’s-related gene, it does not guarantee they will develop the condition. In fact, many people with these gene mutations never develop Parkinson’s at all.
According to the Michael J. Fox Foundation, most people with Parkinson’s do not have a first-degree relative (parent, sibling, or child) with the disease.
Genetic testing may be useful if:
However, genetic testing is not necessary for most people. The results can be complex and often raise more questions than answers. That’s why it’s best to work with a genetic counselor or neurologist who understands movement disorders.
At The Center for Movement Challenges, we can help guide these conversations and connect you with experts if genetic evaluation is appropriate.
While genes are part of the picture, environmental exposures are also important in Parkinson’s risk.
Possible risk factors include:
These factors can interact with a person’s genetic makeup, either increasing or reducing the overall risk of developing Parkinson’s disease.
There is currently no proven way to prevent Parkinson’s disease, but healthy lifestyle habits may help reduce your risk or delay the onset of symptoms.
Some research-backed strategies include:
At The Center for Movement Challenges, our focus on self-care, targeted movement, and early intervention is designed to help people not only live well with Parkinson’s but also reduce their risk of progression.
If you’ve been diagnosed and are wondering what this means for your children or grandchildren, it’s natural to feel anxious. Here’s what we recommend:
We support care partners and families at every stage, with education and personalized guidance for navigating tough conversations.
Wondering is Parkinson’s hereditary can stir up fear. But the truth is, for most people, genetics are just one piece of a much bigger picture. Having a genetic mutation is not a life sentence, and many people with Parkinson’s have no known family history at all.
If you're feeling overwhelmed by questions about Parkinson’s risk, you’re not alone. Our team at The Center for Movement Challenges is here to support you with education, resources, and customized care for every step of your journey.
You are more than your genes — and we’re here to help you live stronger, move better, and worry less.