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Complex regional pain syndrome is a medical condition in which people experience severe pain in parts of the body, such as the limb. However, the pain can spread to other body parts. The symptoms can include stiffness in the affected limb, movement or coordination problems, swelling, muscle spasms, and pain. Vertigo is not a common symptom of this condition.
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Is Vertigo hereditary?
Vertigo can be hereditary but it is more common in men than women!
What are the symptoms of complex regional pain syndrome?
Symptoms can vary, but the most common one is continued pain in any of your limbs. Other symptoms include swelling, sensitivity, stiffness, and changes in the color of the skin.
What are some of the symptoms of menieres disease?
Meniere's disease is a syndrome that affects the inner ear. This means that the most common symptoms will be balance problems and vertigo.
What are the most common symptoms for someone that has vertigo?
Common symptoms for someone that has vertigo are dizziness. also fatigue and nausea. A person with symptoms of vertigo should seek medical attention immediately and refrain from driving.
What is benign positional vertigo?
Benign vertigo is the sudden feeling that you are spinning. This is very common and is not something that should alarm you.
What is the most common nerve entrapment syndrome?
Carpal tunnel syndrome.
How common is Marfan syndrome among other inheritable disorders?
Marfan syndrome is one of the more common inheritable disorders.
What is Angelman's Syndrome's scientific name?
The Scientific name is "Angelman Syndrome" the common name is " Happy Puppet Syndrome"
What is good remedy for virtigo-?
There are many different remedies for Vertigo symptoms. Most common remedies include prescription medications such as Meclizine hydrochloride and Diazepam.
What is the more common name of monosomy X?
Turner syndrome or Ullrich-Turner syndrome.
What chromosome is Proteus syndrome located?
Proteus Syndrome more common in mails or females?
How common is marfan syndrome?
Marfan's syndrome is the most common genetic disorder of connective tissue. It occurs in about every 10,000 to 20,000 individuals.
