A Rare Case Of Huntington’s Disease, Learn About It

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It is hard to see someone close to lose their memory and suffer from brain damage. We are going to discuss one such condition, which might be under a rare condition, but affects a million every year in India. One most important about Huntington’s disease is the fact that it is hereditary.

 

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This affects you if you have had it in your family. You must know if it is present in the family or not. Medications are available to help manage the symptoms of Huntington’s disease, but treatments can’t prevent the physical, mental and behavioral decline associated with the condition.

 

 

You can always book an appointment with doctors online or order medicine online in this case. Visit your doctor regularly to keep yourself in better form and help improve the condition.

 

How do you define Huntington’s disease?

 

Huntington disease is a progressive brain disorder that causes uncontrolled movements, emotional problems, and loss of thinking ability (cognition).

 

Adult-onset Huntington disease, the most common form of this disorder, usually appears in a person’s thirties or forties. Early signs and symptoms can include irritability, depression, small involuntary movements, poor coordination, and trouble learning new information or making decisions. Many people with Huntington disease develop involuntary jerking or twitching movements known as chorea.

 

What are the two types of Huntington disease?

 

These two broad types of this condition that you must know about.

 

1) Adult-onset

 

It is one of the most common of the Huntington disease. It usually appears in a person’s thirties or forties.

 

2) Early-onset

 

This type of Huntington’s disease is less common. Symptoms usually start to appear in childhood or adolescence. Early-onset Huntington’s disease causes mental, emotional, and physical changes.

 

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Detect Huntington disease at an early stage

 

As it is related to the nerves of your brain, an obvious physical symptom is hard to imagine. It happens more in behavior terms. Here are distinguishing symptoms of both.

 

Adult-Onset

 

 

  • Irritability

 

  • Hallucinations

 

  • Psychosis

 

  • Minor involuntary movements

 

  • Poor coordination

 

  • Difficulty understanding new information

 

  • Trouble making decisions

 

Symptoms that may occur as the disease progresses include:

 

  • Uncontrolled twitching movements, called chorea

 

  • Difficulty walking

 

  • Trouble swallowing and speaking

 

  • Confusion

 

  • Memory loss

 

  • Personality changes

 

  • Speech changes

 

  • The decline in cognitive abilities

 

 

Early-onset

 

This type of Huntington’s disease is less common. Symptoms usually start to appear in childhood or adolescence. Early-onset Huntington’s disease causes mental, emotional, and physical changes, such as:

 

 

  • Drooling

 

  • Clumsiness

 

  • Slurred speech

 

  • Slow movements

 

  • Frequent falling

 

  • Rigid muscles

 

 

  • Sudden decline in school performance

 

How do you know that you have Huntington’s disease?

 

To diagnose whether or not you have the disease or not, you must take some tests. Here are the following process and imagine the techniques used by the doctor:

 

  • Neurological Tests

 

  • Brain Function and Imaging Tests

 

  • Psychiatric Tests

 

  • Genetic Testing

 

 

Is there a cause for Huntington’s disease, known?

 

A defect in a single gene causes Huntington’s disease. It’s considered an autosomal dominant disorder. This means that one copy of the abnormal gene is enough to cause the disease. If one of your parents has this genetic defect, you have a 50 percent chance of inheriting it. You can also pass it on to your children.

 

It is not easy to cope with Huntington’s disease if someone you are close to or for that matter a loved one has it. Hence, read the blog carefully and visit our website to know more.

 

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