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Three persons have been identified with Crautzafult-Jacab disease at Hood River County, Oregon.
Creutzfeldt-Jakob Disease (CJD) is a rare and rapid progression brain disorder that belongs to the family of patients, known as printen diseases, also known as transmissible spongeism esfealethis (TSES). (Shutterstock)
In a dangerous health crisis, two people died of a rare, incurable brain disorder, Cretzafalet-Kob disease, within a few months of each other in the Hood River County, in an area of the northwest state of Oregan. Deaths have been reported at a time when county health officials have claimed to identify three cases of cratezfelt-Kob disease in the last eight months.
According to Oregonian, two in three cases have died. While one of them was confirmed by the Autopsy, two other people are diagnosed. It is not yet known whether the cases are related; However, the risk to the public is still “extremely low”, as the Hood River County Health Department monitors the status. “We are trying to look at any common risk factors that can add these cases that can add these cases,” told the outlet, director of the Health Department of Hood River County. But in some cases it is very difficult what the real reason is. ”
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With the monitoring of the health crisis, here you need to know about the rare brain disease.
What is Creutzfeldt-Jakob disease?
Creutzfeldt-Jakob Disease (CJD) is a rare and rapid progression brain disorder that belongs to the family of patients, known as printen diseases, also known as transmissible spongeism esfealethis (TSES).
According to the National Institute of Neurological Disorder and Stroke, the spongeform refers to the way the affected brain views, and with the prinning diseases, the brain is filled with holes and looks like a sponge when examined. CJD causes problems with muscle coordination, thinking and memory. Every year in the US, with the notice of about 350 cases, the CJD moves rapidly, while about 70 percent people die within a year of the disease.
Creutzfeldt-Jakob Causes
A person can develop CJD in various ways, which includes spattified, hereditary or through transmission.
While most cases of CJD are sporadic, where Priyas disease can develop when a person’s normal printer protein suddenly becomes abnormal, it can still be hereditary when gene mutations run in families affecting general prinning protein production.
Creutzfeldt-Jakob disease (CJD) does not spread through air or casual contact. However, it can be transmitted through direct contact of infected brain or nervous system tissues, especially during certain medical procedures.
CJD symptoms
Due to the main symptom of CJD with cognitive decline, it often leads to a lack of coordination in dementia, involuntary muscle shocks and movements. Other early symptoms include poor coordination, running and balance problems, speech difficulty, dizziness, insomnia, vision change, hallucinations, and more. As the situation progresses, individuals can see some other symptoms such as weakness of weapons and legs, blindness, inability to move or speak, problems swallowing and coma.
CJD treatment
There is currently no cure for brain disorders; However, treatment can help relieve symptoms and make the affected person feel comfortable and relaxed. In later stages, patients may need to feed iv fluid and machine.