The difference between cerebral atrophy and cerebellar atrophy.

Written by Zhang Hui
Neurology
Updated on September 04, 2024
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Whether it is cerebral atrophy or cerebellar atrophy, these are concepts in imaging. They are generally detected through cranial CT or MRI scans, resulting in such diagnoses in imaging reports. Generally, cerebral atrophy mainly refers to the atrophy of the cerebral cortex, which includes areas like the frontal lobe, temporal lobe, hippocampus, and parietal lobe. The cerebral cortex is closely related to cognitive functions, movement, sensation, and emotions of the limbs. Patients with cerebral atrophy typically show a decline in intelligence, slow reactions, and dysfunction of bladder and bowel control, etc. The cerebellum mainly coordinates the body's integrative movements and ensures the fluent execution of limb movements. Therefore, cerebellar atrophy primarily leads to symptoms of ataxia, like finger tremors and unsteady walking.

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Written by Zhang Hui
Neurology
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Is cerebellar atrophy hereditary?

Whether cerebellar atrophy is hereditary depends on the cause of the atrophy. In neurology, there is a disease called spinocerebellar ataxia, which is caused by genetic mutations and results in significant ataxic symptoms. The imaging studies show cerebellar atrophy. This disease can be inherited, so it is important to conduct prenatal counseling to promote eugenics. Cerebellar atrophy caused by other reasons is not hereditary. For example, if the atrophy is due to neurodegenerative disease such as multiple system atrophy, there is no clear genetic tendency. If the atrophy is caused by a cerebellar infarction, it is also not hereditary.

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Written by Zhang Hui
Neurology
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Symptoms of cerebral atrophy

Mild cerebral atrophy may not present any clinical symptoms, and many elderly people show some degree of cerebral atrophy during imaging examinations, which should not be overly worrying. If the cerebral atrophy is more pronounced, it mainly manifests as cognitive dysfunction, such as a decline in memory, reduced computational abilities, diminished executive functions, and possibly the inability to perform complex movements, such as being unable to brush one's teeth or dress oneself. In severe cases, individuals may experience personality changes, becoming irritable, easily angered, suspicious, and may even exhibit psychiatric symptoms, primarily hallucinations.

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Written by Zhang Hui
Neurology
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Can cerebellar atrophy be cured?

Cerebellar atrophy is difficult to cure. There are many causes of cerebellar atrophy, such as degenerative diseases of the nervous system. For example, olivopontocerebellar atrophy, which is caused by a disease with an unknown pathogenesis leading to the death of cerebellar cells and resulting in atrophy, currently lacks effective treatment methods and is incurable. Some cases are due to hereditary diseases, such as spinocerebellar ataxia, where patients also suffer from cerebellar atrophy, making it very difficult to cure. In addition, some patients who have been chronically drinking alcohol can also develop cerebellar atrophy due to alcohol poisoning. Although clinical symptoms can be significantly improved by discontinuing alcohol use and administering large amounts of vitamin B1 and B12, the atrophy in the cerebellum cannot be reversed as seen on imaging studies.

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Written by Li Jiao Yan
Neonatology
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Symptoms of baby brain atrophy

The symptoms of baby brain atrophy include the following: First, the child shows no interest in the surroundings, poor responsiveness, significantly reduced movements, poor sucking ability, and often chokes on milk. Second, the child with brain atrophy exhibits abnormal muscle tone and posture. Symptoms of cerebellar atrophy include difficulty in abducting the thighs, difficulty in extending the knees, legs straightened and adducted when held upright, legs crossed in a scissor-like manner, bent elbow and wrist joints, and the hands often clenched with the thumb turned inward. Third, congenital reflexes are weakened or may not appear at all, such as the rooting reflex, grasp reflex, and embrace reflex, which are either weakened or completely absent. Fourth, there is limited voluntary movement; the baby cannot reach out voluntarily to grab liked objects after five months or always uses one hand to reach for things. Fifth, there are signs of intellectual disability, delayed language development, or language disorders.

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Written by Zhang Hui
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Does brain atrophy cause dizziness?

If it is brain atrophy, generally it does not cause dizziness; patients with mild conditions may not show any clinical symptoms. If it is severe, the main symptoms are those of dementia, such as possible sluggish reactions, memory decline, reduced computational abilities, impaired executive functions, and even psychiatric symptoms. The most common disease clinically observed is Alzheimer's disease. If the patient has cerebellar atrophy, even mild cases might not exhibit any symptoms. Severe cases can experience dizziness, primarily manifesting as feeling drunk, accompanied by unsteady walking, unstable standing, and other signs of ataxia.