Is brain atrophy hereditary?

Written by Zhang Hui
Neurology
Updated on September 21, 2024
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There are many causes of brain atrophy; whether it is hereditary depends on the specific disease causing it. Most diseases leading to brain atrophy are not hereditary. For instance, some patients suffer brain atrophy due to Alzheimer's disease, where the neurons die irreversibly. This disease is mostly sporadic and does not have a clear hereditary tendency. Of course, a few cases of Alzheimer's do have a family history and may have a genetic propensity. Additionally, brain atrophy can also occur due to intoxication, such as from alcohol, carbon monoxide, or other toxic substances, and these cases definitely are not hereditary. Some patients experience brain atrophy due to cerebral thrombosis, which also lacks a genetic predisposition.

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Written by Zhang Hui
Neurology
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Do elderly people with brain atrophy experience dizziness?

If a patient exhibits atrophy of the cerebral cortex, elderly individuals generally do not show clinical symptoms of dizziness. The main manifestations are cognitive impairments, such as a decline in memory, computational ability, and judgment, as well as decreased executive functions. Some severe cases may even show personality changes and exhibit mental symptoms. If the patient has significant cerebellar atrophy, it is possible for them to experience dizziness, such as in cases of multiple system atrophy causing cerebellar atrophy, where the elderly may notably suffer from dizziness, which is related to changes in body position, particularly making them prone to dizziness when standing.

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Written by Bian Jun Li
Neurology
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Cerebellar atrophy symptoms

The main functions of the cerebellum include maintaining bodily balance, controlling posture and gait, regulating muscle tone, and coordinating the accuracy of voluntary movements. Therefore, the primary symptoms of cerebellar atrophy involve ataxia, with patients displaying instability in standing, a staggering gait similar to that of a drunken walk; speech may manifest as cerebellar speech, or a chanting-like pattern; there can also be disorders in fine motor skills, where some precise movements cannot be accurately performed, and coarse movements may sometimes not be severely affected; additionally, there can be disturbances in eye movement, presenting as tremors of both eyes, and patients may experience symptoms of vertigo clinically.

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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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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 Jian Wu
Pulmonology
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Brain atrophy should be treated in the neurology department.

Cerebral atrophy is a type of vascular pathology. Patients need to visit the neurology department of a hospital for examination. Mild cases may lead to a decline in memory, while severe cases can affect intelligence and the ability to live normally. Patients with mild symptoms should timely follow medical advice to choose medications that nourish brain cells, and should also stabilize blood pressure, blood sugar, and blood viscosity. Engaging in intellectual games, exercising brain cells, having family companionship, participating in outdoor exercises to enhance immune capabilities, stabilizing the condition, and undergoing regular follow-ups are also advised.