6-year-old girl suddenly can't walk, experts say, it is related to genes!

According to the Minsheng Channel of Henan TV, a 6-year-old girl in Henan suddenly couldn't walk, her legs twitched and trembled, and her father took her around in a cart every day to find a docto.

A doctor from the Department of Neurology at Henan Maternal and Child Health Hospital said that the child has no sensory impairment, only motor impairment, and both of M.

What is Spinocerebellar Atrophy? With what factors?

Cerebellar atrophy, also known as spinocerebellar atrophy, is a familial genetic disorder of the nervous syste.

Of course, not all cerebellar atrophy is hereditar.

Cerebral ischemia and cerebral hemorrhage

Causes the blood supply to decrease and the nerve cells die, resulting in atrophy of the cerebellum;

Multiple system atrophy

This is a degenerative disease that affects the whole body and may be related to genetics, exposure to heavy metals, toxic organic solvents,et.

Other

Multiple sclerosis, tumors, chronic alcoholism, and genetic factors may also cause cerebellar atroph.

What does spinocerebellar atrophy look like? How to treat?

Cerebellar atrophy can be divided into three stages:

In the first stage, the initial symptoms are as if drunk when walking, uncoordinated movements up and down stairs, body shaking back and forth when standing, dizziness and other symptom.

In the second stage, the mid-term symptoms will appear uncontrollable support and gait, walking like a penguin, eating and drinking, choking, slurred speech and other symptom.

In the third stage, in the late stage, there will be extremely unclear language, unable to control the pitch or even unable to speak, unable to recognize when writing, completely unable to walk, difficulty swallowing and other symptom.

At present, there is no effective treatment for cerebellar atrophy, and interventions are mainly aimed at some controllable pathogenic factor.