Is there any End to Huntington’s disease?


Huntington’s disease is a fatal genetic disorder that causes the tolerant breakdown of nerve cells in the brain. It deteriorates a person’s physical and mental abilities during their prime working years and has no cure. Nowadays there are approximately 30,000 suggestive Americans and more than 200,000 at-risk of causing the disease.

Symptoms the initial age is 30 to 50 and it gets chronic in the period between 10 to 25 year. Ultimately, the weakened individual causes to pneumonia, heart failure or other complications. Everyone has the gene that causes Huntington’s disease, but only Huntington’s disease and possibly pass it on to upcoming those that inherit the expansion of the gene will get the generation.

Symptoms Include:

Personality changes, mood swings & depression
Forgetfulness & impaired judgment
Unsteady gait & involuntary movements (chorea)
Slurred speech, difficulty in swallowing & significant weight loss

Who Is At Risk

Every child of a parent with Huntington’s disease has a 50/50 chance of receiving the expanded gene that causes the disease. If the child has not inherited this expanded gene, he or she will never develop the disease and cannot pass it on to their children.






Research

For the first time ,A system to model embryonic  stem cell have been developed by scientist  by introducing  early abnormalities in the way Huntington’s neurons look, and how these cells form larger structures that had not previously been associated with the disease.
Huntington’s is straight frontward genetic culprit diseases. Total hundred percent of people having mutated Huntington (HTT) form of the gene for developing the diseases. Extra DNA is taken by mutation to produce longer protein then usual protein by the gene
Researchers hope that these new cells will be a further useful for studying the cellular and molecular convolutions of Huntington’s disease and suggested a new model  for humans which will be further useful for the brain and other diseases
                 

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