Tay-Sachs is a deadly disease

• April 28, 2024

Tay-Sachs is a disease mortal that is generated in the nervous system of the human being and transmitted by inheritance genetics, when both parents provide a defective gene chromosome 15.

It occurs regularly when the body lacks hexosaminidase A, which is a protein responsible for destroying the fatty components present in the nerve cells .

It is divided into three stages: the infantile, the juvenile and late start. However, most people present the first phase, that is, when the neurological damage begins when the baby is inside the uterus , but the symptoms appear at three or six months of age; the condition progresses rapidly and the infant dies at 4 or 5 years.

According to the National Tay-Sachs & Allied Diseases , among the most common symptoms of this disease they find each other:

1. Deafness
2. Blindness
3. Loss of muscle strength
4. Delay in the development of mental and social skills
5. Dementia
6. Irritability
7. Apathy
8. Epileptic seizures
9. Loss of motor skills

According to experts there is no treatment for the condition, only some therapies to help the patient and their relatives.

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Video Medicine: Tay-Sachs Disease ¦ Treatment and Symptoms (April 2024).