Hereditary movement disorder difficulty standing up is caused by these diseases

Difficulty standing up due to hereditary movement disorders mainly refers to the patient's postural balance disorder, unstable gait, leaning backward or to one side, etc., and they are unable to stand normally. Studies have found that the causes of this disease are commonly found in cerebrovascular diseases, tumors, inflammation, trauma, degenerative diseases, etc. in the frontal lobe, parietal lobe, facial lobe, occipital lobe, and dirty body parts of the brain.

1. Basic Content

There are three types of cerebral ataxia:

1. When frontal lobe ataxia occurs due to lesions in the frontal lobe or frontopontocerebellar tract, the symptoms are similar to cerebellar ataxia, such as postural balance disorder, unstable gait, and falling backward or to one side. In addition to contralateral limb ataxia, it is often accompanied by hyperreflexia, increased muscle tone, positive pathological reflexes, as well as mental symptoms, strong grip reflex, and tonic plantar reflex, which are manifestations of frontal lobe damage.

2. Parietal ataxia manifests itself as varying degrees of ataxia in the contralateral affected limb, which is obvious when the eyes are closed. Deep sensory impairment is usually mild or transient. Damage to the posterior part of the paracentral lobules on both sides may cause sensory ataxia of both lower limbs and urinary and bowel disorders.

3. Temporal lobe ataxia is mild and may manifest as transient balance disorders, which is not easy to detect early.

2. Causes

Commonly seen in cerebrovascular diseases, tumors, inflammation, trauma, degenerative diseases, etc. in the frontal lobe, parietal lobe, facial lobe, occipital lobe, dirty body and other parts of the brain.

3. Prevention

The prevention of hereditary ataxia mainly depends on genetic counseling, but because these diseases have multiple inheritance modes, genetic counseling is still difficult. Therefore, prevention is mainly to avoid consanguineous marriage; for members with a family history, they should go to the hospital for regular check-ups starting from childhood to detect any ataxia symptoms such as bone deformities, eye symptoms, heart disease, and unsteady walking as early as possible, so that early treatment can delay the progression of the disease or prolong the period of static stability.