The Greater Solutions for the Huntington’s disease


Formerly known as Saint Guy’s Dance, Huntington’s disease is a degenerative, rare and hereditary neurological disease. It appears from birth or much later, between 35 and 50 years; very rarely, it can occur in people aged 15 to 25 years. It is caused by degeneration of neurons and reaches the sub-cortical area of ​​the brain.

What are the symptoms of Huntington’s disease?

Many symptoms accompany Huntington’s disease: 

Physical symptoms:

  • Involuntary movements and spasms of the head, neck and all limbs. These movements are jerky type. They are often accompanied by episodes of loss of balance, lethargy and coordination disorders.

Psychological symptoms

  • Mental disorders, depression, abnormal irritability, disorientation and some anxiety. This results in a gradual degradation of cognitive functions leading to dementia in the final stage of the disease.

Frequent complications:

  • Various infections such as pneumonia and pulmonary embolism. In the majority of cases, these complications unfortunately cause death about fifteen years later.

How to diagnose Huntington’s disease?

The symptoms of Huntington’s disease being often variable from one patient to another and very similar to those of a person with purely psychological disorders, the diagnosis of Huntington’s disease is very difficult to ask.

The doctor will perform tests of the neuropsychological type to measure the loss of cognitive functions but only an MRI or a genetic test, will confirm this diagnosis with certainty.


What are the causes of Huntington’s disease?

In one in 10,000 people, Huntington’s disease is caused by an abnormality at the genetic level, localized at chromosome 4. This anomaly consists of an abnormal repetition of certain DNA triplets on this chromosome. This anomaly is said to be of the autosomal dominant type, that is, its existence on only one of the two chromosomes already causes the disease.

What tests to diagnose Huntington’s disease?


There are different tests to highlight Huntington’s disease:

Perform a brain scan to check for possible atrophy of the coded nuclei and the frontal lobe of the brain. This atrophy, as well as the dilatation of the frontal horns constitutes the irrefutable proof that it is indeed Huntington’s disease. Neuropsychological tests are also carried out to measure the evolution of the disease by testing the cognitive faculties. This is the reason that at present the use of Balance CBD comes useful in every possible manner.

What are the symptoms of Huntington’s disease?

There is a wide variety of significant symptoms of Huntington’s disease and not all individuals necessarily present them to the same degree. Nevertheless, there are 3 main symptoms that are indicative of Huntington’s disease:

Physical symptoms:

  • Involuntary movements,
  • Clumsiness,
  • Balance disorders
  • Difficulties to articulate.

Emotional symptoms:

  • Depression,
  • Irritability,
  • Personality modification,
  • Psychosis

Cognitive symptoms:

  • Loss of memory,
  • Loss of attention,
  • Difficulty making decisions

Learn more about these symptoms:

All of these symptoms will be different in different individuals. Some, for example, will experience great difficulties associated with involuntary movements, while others will have few physical symptoms but will face many emotional or cognitive difficulties.

What are the different stages of Huntington’s disease?

The first symptoms of Huntington’s disease are mild physical changes and possibly cognitive or emotional changes to gradually progress to the advanced stage of the disease.