What is corticobasal degeneration?
Corticobasal degeneration (CBD) is a rare neurological disorder that causes degeneration of the motor and cognitive parts of the brain.
What are the first symptoms of corticobasal degeneration?
The first symptoms of corticobasal degeneration can vary, but they often include problems with movement, such as stiffness or difficulty controlling muscles on one side of the body.
What are the final stages of corticobasal degeneration?
The final stages of corticobasal degeneration are characterized by severe motor and cognitive impairment, difficulty swallowing, and an increased risk of pneumonia due to aspiration of food and liquids.
What causes corticobasal degeneration?
The exact cause of corticobasal degeneration is unknown, but it is believed to be caused by the accumulation of abnormal proteins in the brain known as tau protein.
Is corticobasal degeneration hereditary?
There is no known genetic component to corticobasal degeneration, but some cases have been reported in families with a history of the disease.
What are the symptoms of corticobasal degeneration?
Symptoms of corticobasal degeneration include stiffness and difficulty controlling muscles, tremors, muscle jerks, difficulty with speech and swallowing, and cognitive decline.
What is the corticobasal degeneration survival rate?
The average survival rate for corticobasal degeneration is 6-8 years from the onset of symptoms.
What is corticobasal degeneration syndrome?
Corticobasal degeneration syndrome is a clinical diagnosis in which a person has the symptoms of corticobasal degeneration without a confirmed diagnosis via MRI or biopsy.
What is the corticobasal degeneration timeline?
The timeline of corticobasal degeneration can vary, but it typically progresses slowly over the course of several years, with symptoms worsening over time.
What is the end of life like for someone with corticobasal degeneration?
The end of life for someone with corticobasal degeneration is often marked by severe motor and cognitive impairment, difficulty swallowing, and an increased risk of pneumonia due to aspiration of food and liquids.
Are there corticobasal degeneration clinical trials currently underway?
Yes, there are currently several clinical trials underway to evaluate potential treatments for corticobasal degeneration.
What is the corticobasal degeneration treatment?
There is no known cure for corticobasal degeneration, but treatment options may include medications to control symptoms and physical therapy to improve mobility and function.
What is corticobasal ganglionic degeneration?
Corticobasal ganglionic degeneration is a subtype of corticobasal degeneration that also involves degeneration of the basal ganglia, which plays a key role in movement control.
What are some corticobasal degeneration stories?
There are many stories of individuals and families affected by corticobasal degeneration, each with their own unique experiences and challenges.
What can an MRI reveal about corticobasal degeneration?
An MRI can reveal atrophy or shrinkage of the affected areas of the brain, which can help confirm a diagnosis of corticobasal degeneration.
What is the ICD-10 code for corticobasal degeneration?
The ICD-10 code for corticobasal degeneration is G23.1.
What are the corticobasal degeneration stages?
The stages of corticobasal degeneration can vary, but typically progress from mild symptoms such as tremors and stiffness to severe motor and cognitive impairment.
Is there a cure for corticobasal degeneration?
There is no known cure for corticobasal degeneration at this time.
What treatment options are available for corticobasal degeneration?
Treatment options for corticobasal degeneration may include medications to control symptoms, physical therapy, and speech therapy.
What are the long-term effects of corticobasal degeneration?
The long-term effects of corticobasal degeneration include severe motor and cognitive impairment and an increased risk of pneumonia due to aspiration of food and liquids.
What is the prognosis for corticobasal degeneration?
The prognosis for corticobasal degeneration is poor, with an average survival rate of 6-8 years from the onset of symptoms.
Is there a cure for corticobasal ganglionic degeneration?
There is no known cure for corticobasal ganglionic degeneration at this time.
What are the differences between corticobasal degeneration and Parkinson's disease?
Corticobasal degeneration and Parkinson's disease share some similarities in terms of symptoms, but corticobasal degeneration typically progresses more quickly and affects a wider range of motor and cognitive functions.
Can corticobasal degeneration be prevented?
There is currently no known way to prevent corticobasal degeneration.
Are there any alternative therapies or treatments for corticobasal degeneration?
There is currently no evidence to support the use of alternative therapies for corticobasal degeneration.
What is the life expectancy for someone with corticobasal degeneration?
The life expectancy for someone with corticobasal degeneration is typically 6-8 years from the onset of symptoms.
What is the role of tau protein in corticobasal degeneration?
Tau protein is thought to accumulate in the affected areas of the brain in corticobasal degeneration, leading to the degeneration of these areas and the symptoms associated with the disease.
What are the risk factors for corticobasal degeneration?
The exact risk factors for corticobasal degeneration are unknown, but some cases have been reported in families with a history of the disease.
What are the chances of developing corticobasal degeneration?
Corticobasal degeneration is a rare disease, with an estimated prevalence of 1-2 cases per 100,000 people.
What are the similarities and differences between corticobasal degeneration and progressive supranuclear palsy?
Corticobasal degeneration and progressive supranuclear palsy share some similarities in terms of symptoms and progression, but there are also some key differences in the areas of the brain that are affected.
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