If you or someone you care about is having trouble walking or seems uncoordinated or clumsy, limb ataxia may be the cause. This neurological condition, which can be inherited or related to an underlying condition, causes issues with balance, coordination, and muscle control.
If you have limb ataxia, you may also notice you make awkward movements and have tremors, especially when trying to write, eat, or type. This can make day-to-day life more challenging and can negatively impact your overall quality of life.
That’s why it’s so important to know the symptoms, causes, and treatment for limb ataxia. Being armed with this information can help you understand what to expect and advocate for the medical care you need.
If you have limb ataxia, you may feel like your movements are awkward or clumsy. You may notice tremors in your arms and legs, especially when you’re trying to do a specific task. This condition can also affect the way you walk and make fine motor tasks like writing or typing more challenging. Here are some common symptoms associated with limb ataxia:
Those with limb ataxia who use a wheelchair are also at an increased risk for pressure sores, blood clots, and skin infections. So, if you use a wheelchair, it’s important to watch for these symptoms as well.
Limb ataxia is a degenerative condition that is caused by damage to your cerebellum, the part of your brain that controls movement. People with this condition may have trouble walking, stumble and fall, or appear uncoordinated.
There are several different reasons why someone might develop limb ataxia, including genetic causes or other health conditions like vitamin deficiencies or autoimmune disorders. Limb ataxia may also be sporadic or idiopathic, meaning there is no known cause.
Here’s what you need to know about the potential causes of limb ataxia.
If you have hereditary limb ataxia, this means the genes you inherited from your parents played a role in its development. Inherited limb ataxia can run in families and is either dominant or recessive.
If you have a dominantly inherited limb ataxia, this means it may be caused by a mutated gene passed from only one parent.
If you have a recessively inherited limb ataxia, this means you received a copy of the defective gene from each parent. In this case, your parents are considered carriers of the condition.
When parents are carriers, each child has a 25 percent chance of developing the disease, a 25 percent chance of inheriting no ataxia genes, and a 50 percent chance of becoming a carrier themselves. This is why ataxia can be passed on for generations even though there may seem to be no family history of the condition.
Some examples of dominant ataxias include spinocerebellar ataxia and episodic ataxia. Meanwhile, recessive ataxias include ataxia-telangiectasia, Friedreich ataxia, and mitochondrial ataxia.
If you have an acquired limb ataxia, this means there’s an external cause for the condition or that something other than your genes has affected your brain. This can include a wide range of conditions, from alcohol abuse to an autoimmune disease. Here are some common causes of an acquired ataxia:
When you develop limb ataxia that’s not inherited or caused by something external like an underlying condition, your healthcare provider may diagnose you with sporadic limb ataxia, which means there’s no known cause for the condition. Usually, this type of limb ataxia is hard to diagnose because other forms of ataxia have to be ruled out.
Sometimes physicians will label the condition pure cerebellar, which means only the cerebellum is affected, or cerebellar plus, meaning you have additional symptoms such as neuropathy (nerve damage), dementia (mental decline), and weakness in addition to muscle spasms and stiffness.

Often, the treatment for ataxia depends on what’s causing it to begin with. For ataxias caused by something in your environment — like those related to gluten, alcohol, medications, or infections — your healthcare provider will address the root cause by, for example, treating the infection, removing gluten from your diet, or changing your medication. If you stick to the treatment, your limb ataxia may go away.
If you have limb ataxia that is caused by a genetic condition like Friedreich ataxia or an underlying condition like Huntington’s disease or multiple sclerosis (MS), your ataxia will likely need to be managed with therapies, assistive devices, and medications. For instance, if you have Friedreich ataxia, you may be prescribed omaveloxolone (Skyclarys), which may improve your symptoms.
Here are some other ways that limb ataxia may be managed or treated:
If you develop symptoms of limb ataxia, a healthcare provider will likely take your medical history and do a physical exam. They may also ask you if anyone in your family has the condition and take note of what medications you’re taking and how much alcohol you drink, since both can cause limb ataxia in some people. After this initial exam, they may order testing to further help them make a diagnosis.
Possible tests include:
On MyAtaxiaTeam, people share their experiences with ataxia, get advice, and find support from others who understand.
Have you or a loved one developed symptoms of limb ataxia? Let others know in the comments below.
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