a CLINICAL Experience
Simply put, a diagnosis is described as “clinical,” it means this: It’s based on expert observation and pattern recognition—not a single test.
For Parkinson’s, there is no blood test, scan, or lab result that can definitively confirm the diagnosis on its own.
Instead, a clinician—usually a neurologist—use:
Think of it like this:
A lab or imaging test is a snapshot.
A clinical diagnosis is the movie.
These observations often reveal patterns that structured tests alone can’t—and help guide the rest of the exam.
The exam should include a review of your medical history, along with your symptoms and how they’ve changed over time. When symptoms began, how they’ve progressed, and what makes them better or worse all provide important context and help the neurologist interpret what they see during the exam.
While these tasks may seem straightforward, the neurologist is observing several subtle details at the same time. They are looking for slowing as the movement continues, a gradual decrease in movement size or amplitude, hesitation when starting or stopping, and fatigue that appears with repetition. Consistency matters as much as speed.
Importantly, this isn’t about how fast you move at the start—it’s about how movement changes over time. These patterns help distinguish Parkinson’s-related bradykinesia from normal slowing, stiffness, or weakness.
The goal is to assess muscle tone, not strength. As your limbs are moved, the neurologist is feeling for resistance to passive movement—a hallmark feature of Parkinson’s disease.
They are specifically looking for:
The neurologist may repeat these movements or ask you to perform a simple task with the opposite limb (such as opening and closing your hand) to see if rigidity becomes more apparent, a phenomenon known as activation.
Importantly, rigidity in Parkinson’s is different from spasticity or joint problems. These findings help the neurologist distinguish Parkinson’s disease from other neurologic or musculoskeletal conditions.
The neurologist is assessing the timing, pattern, and distribution of the tremor. Parkinson’s tremor most often appears at rest and may decrease or temporarily disappear with movement, while other tremor types—such as essential tremor—are more prominent during action or posture.
These details help distinguish Parkinson’s-related tremor from essential tremor and other neurologic conditions. Importantly, not everyone with Parkinson’s has a visible tremor, and the absence of tremor does not rule out the disease.
While you perform these tasks, the neurologist is observing multiple features at once. They are assessing stride length, walking speed, foot clearance, and whether steps become shorter or shuffling. Turning style is closely watched, including whether you pivot smoothly or need several small steps to change direction.
They also look for:
Posture, including forward stooping or stiffness
Arm swing, which is often reduced or asymmetric in Parkinson’s
Balance responses, especially how quickly and effectively you recover when gently pulled backward
Hesitation or freezing when starting, stopping, or turning
These features can be subtle and are often noticed more by others than by the person experiencing them.
In addition to what can be observed, the neurologist will ask targeted questions about non-motor symptoms, which are an important part of Parkinson’s disease and often appear years before movement changes. These may include:
These non-motor features provide critical context and help support the diagnosis, even when motor symptoms are mild. Together with the movement exam, they help the neurologist identify a consistent pattern rather than relying on any single finding.
A movement-disorder neurologist is not looking for one isolated sign. They are looking for a pattern of features that fit together, including:
Just as important is what doesn’t appear during the exam or on supporting tests. Normal imaging or lab results don’t rule out Parkinson’s—they often help confirm that symptoms aren’t caused by something else.
For many people, diagnosis doesn’t happen in a single visit. It often unfolds over multiple appointments, as patterns become clearer and changes over time provide additional insight. This step-by-step approach is intentional—and it’s one of the reasons experience with Parkinson’s matters.
There is no blood test that confirms Parkinson’s Disease. These tests are used to exclude other conditions that can look similar, helping clinicians narrow the diagnosis through a process of elimination.
Commonly tested genes include:
LRRK2 – the most common genetic cause of Parkinson’s worldwide
GBA – increases risk and may influence symptom progression
PARK2 (Parkin) – often linked to younger-onset Parkinson’s
PINK1 – associated with early-onset forms
SNCA – rare, but directly involved in Alpha-Synuclein production
These panels focus only on genes with established relevance, rather than sequencing everything.
A Biomarker is a measurable substance or characteristic in the body that provides information about health or disease.
Example:
High cholesterol is a Biomarker that signals increased risk for heart disease.
Biomarkers can be found in blood, urine, cerebrospinal fluid, skin, or tissue.
For Parkinson’s, Biomarker research is still evolving, but it is becoming increasingly important for improving diagnosis, research, and clinical trials.
Biomarker tests do not diagnose Parkinson’s on their own, but they can give healthcare providers additional clues. Two emerging tests you may hear about are the Alpha-Synuclein Seed Amplification Assay (SAA) and the Syn-One Skin Biopsy Test. Both look for abnormal forms of the protein Alpha-Synuclein, a key protein involved in Parkinson’s Disease.
As mentioned, Parkinson’s is diagnosed based on clinical judgment, not a single test. Biomarkers like SAA and Syn-One represent promising tools that may improve diagnostic confidence and research, but they are supporting pieces of the puzzle, not standalone answers.