- What Is
What is Cotard’s syndrome?
Cotard’s syndrome, also known as walking corpse syndrome, is a neuropsychiatric condition in which people develop false beliefs that their body parts are missing, or they are dying or they don’t exist. This condition is rare because only 200 known cases are present worldwide.
What are the symptoms of Cotard’s syndrome?
People with Cotard’s syndrome manifest the following symptoms:
What is the cause of Cotard’s syndrome?
The exact cause of Cotard’s syndrome is unknown. There are certain conditions that more likely cause this syndrome:
- Dementia (loss of memory and judgment)
- Encephalopathy (a condition, where a virus or toxin affects the brain)
- Multiple sclerosis (serious disabling disease of the brain and spinal cord)
- Parkinson’s disease (nerve cell damage in the brain leading to shaking, stiffness and gait difficulty)
- Subdural bleeding (bleeding outside the brain)
Who is at the risk of getting Cotard’s syndrome?
People in their early 50s are at the risk of getting Cotard’s syndrome. People with the following conditions are at higher risk:
How is Cotard’s syndrome diagnosed?
Because Cotard’s syndrome is not a disease, it doesn’t have standardized diagnostic criteria. The physician may rule out other conditions to confirm the diagnosis of Cotard’s syndrome. The physician might ask about the symptoms or any risk factors.
How is Cotard’s syndrome treated?
These therapies can treat Cotard’s syndrome to a great extent.
Medications used to treat Cotard’s syndrome include the following:
- Antianxiety drugs
Electroconvulsive therapy (ECT) can be the preferred choice of therapy in the case of failed medication and talk therapy. ECT therapy involves sending small currents through the brain. This alters the brain’s chemistry to relieve some of the symptoms.
Is Cotard’s syndrome curable?
Although the symptoms are severe, Cotard’s syndrome is curable with treatment. Generally, electroconvulsive therapy (ECT) therapy is beneficial compared to medications in treating Cotard’s syndrome.