The Arnold-Chiari syndrome is a rare malformation of the brain. See also the link below.
Chiari malformation is curable by surgery.
chiari affects 1 in 1,000 people.
Yes, there is evidence to suggest that Arnold-Chiari Malformation may have a hereditary component, but the exact genetic factors involved are still under investigation. It is believed that genetic mutations may play a role in predisposing individuals to developing this condition.
An AVM is an arteriovenous malformation, so it is a malformation that connects arteries and veins, while a Chiari Malformation (more commonly referred to as an Arnold-Chiari Malformation) is one where part of the brain herniates (pushes through) the base of the skull.
Yes, it is a hereditary disease.
Long-term prognosis for persons with Arnold-Chiari I malformations is excellent. Full recovery from surgery may take several months.
yes.
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The exact cause is still known. It is known to run in some families.
One of the most common symptoms of Arnold-Chiari malformations is a headache . The headache generally begins in the neck or base of the skull and may radiate through the back of the head.
Arnold-Chiari malformation is a condition where the brain tissue extends into the spinal canal. This can disrupt the flow of cerebrospinal fluid, causing symptoms like headaches, dizziness, and difficulty walking. Treatment may involve surgery to relieve pressure on the brain and spinal cord.