health conditions Post

Effects of Huntington’s disease

Huntington’s chorea is an inherited condition that results in the progressive degeneration of the brain cells, which affects mobility and thinking and exhibits psychiatric symptoms. Usually, the symptoms are seen in an individual between the age of 30 and 40 years, but they can be seen later or earlier as well. When the symptoms manifest before the age of twenty, it is called juvenile Huntington’s disease. An earlier emergence has faster progression and showcases different symptoms. There are medicines that keep a check on the symptoms related to the disorder, but the cognitive, physical, and mental degradation has no medicine as of now. Movement disorders Huntington’s Chorea affects both voluntary and involuntary movements, but impairment of voluntary movement will have more effect as it can interfere with the day-to-day life. Some of them are as follows: Jerking or writhing involuntarily Eye movements becoming slow and abnormal Muscles behaving improperly by being rigid Being unable to balance the body and having an abnormal gait and posture Difficulty in speaking and swallowing food Cognitive disorders Cognitive disorders associated with Huntington’s chorea are as follows: Difficulty in planning and organizing things Lack of clarity and often getting stuck with one thought Lack of impulse leading to sudden emotional outburst and sexual promiscuity Slow in finding the right word while carrying out conversations Difficulty in learning new things Psychiatric disorders Depression is the most common disorder that is associated with psychiatric disorders.