Parkinson’s disease is a disorder of the nervous system. It is a progressive condition and causes widespread degeneration within the brain.
Approximately 15% of people diagnosed with Parkinson’s disease have a known family history of the disorder. Genetic inheritance is considered a major risk factor. Biological interactions that give rise to Parkinson’s are complex and not fully understood.
Parkinson’s disease often begins with trembling or shaking of a body part, especially when at rest. Symptoms are usually more pronounced across one half of the body, with many patients noticing it in the hand. It can also affect arms, legs, feet, and the face.
Additional symptoms emerge over time. These include:
Not all patients experience every symptom in the early stages. As it progresses, however, most patients will encounter all of the characteristic symptoms above.
Parkinson’s patients should be monitored for signs of dementia, a decline of judgment, and memory. The likelihood of dementia increases according to patient age.
Children do not inherit Parkinson’s disease directly from their parents. However, a parent’s history of the disease makes it more likely that a child may experience it later on in life. It is important to remember that genes represent a probability, not a definite outcome.
People who lack a family history of Parkinson’s sometimes develop the condition. Environmental factors play a role in whether pertinent genes activate. However, the precise triggers remain unknown.
Family history is the most significant risk factor for Parkinson’s disease. Other risk factors include:
Men are more likely to experience Parkinson’s disease than women.
Only about 5% of those with Parkinson’s are diagnosed before 60.
Genes associated with Parkinson’s include, but may not be limited to:
Several recessive genes may also play a role. Recessive genes may be carried by an individual who does not have the specific health condition associated with the gene. Parkinson’s is an example, and it becomes more likely if recessive genes are received from both parents.
The recessive genes associated with Parkinson’s are:
Currently, there are no medications or procedures that will prevent genetic Parkinson’s disease. Not all of the genes involved in Parkinson’s have been identified at this time.
Likewise, the environmental factors that may make them active have not been isolated.
If you know that you have a family history of Parkinson’s disease, discussing the matter with your doctor is an important first step. Your doctor will help you determine whether genetic testing can help you understand your risk factors better.
To learn more about Parkinson’s Disease, contact Complete Neurological Care.