Wilson’s disease is a rare genetic disorder that causes copper to accumulate in the body, affecting the liver, brain, and other organs. This build-up of copper can lead to symptoms such as jaundice, fatigue, abdominal pain, and neurological issues. If left untreated, Wilson’s disease can be life-threatening. The good news is that Wilson’s disease is […]
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Williams syndrome is a rare genetic disorder that affects around 1 in 10,000 people worldwide. It is caused by a deletion of genetic material from chromosome 7, resulting in a range of developmental and medical problems. There is currently no cure for Williams syndrome, as it is a genetic disorder. However, there are treatments available
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White matter heterotopia is a rare neurological condition characterized by the presence of abnormally located clusters of white matter in the brain. This condition is typically present from birth and may be associated with other neurological abnormalities or developmental delays. White matter heterotopia can be diagnosed through neuroimaging studies such as MRI or CT scans.
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West syndrome, also known as infantile spasms, is a rare type of epilepsy that typically begins in the first year of life. It is characterized by a specific type of seizure called infantile spasms, as well as developmental regression and a distinctive pattern on electroencephalogram (EEG) testing. While there is currently no cure for West
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West Nile virus encephalitis is a potentially serious neurological disease caused by the West Nile virus. The virus is typically spread through the bite of an infected mosquito and can lead to inflammation of the brain (encephalitis) or the membranes surrounding the brain and spinal cord (meningitis). Many people infected with the virus do not
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