Is otolithiasis caused by low body resistance?

1. Genetic factors.

Genetic factors can cause otolithiasis. Data shows that about 54% of people have a family history of the disease. Especially in first-degree families, the risk of this disease is higher.

In the body of otolithiasis patients, many people suffer from otolithiasis due to certain secret inheritance of chromosomes, and genetic mutations are also very common causes.

2. Endocrine disorders.

Otolithiasis is related to endocrine disorders. It usually occurs in younger people, is more common in women, and accelerates during pregnancy, childbirth, and menopause. This condition is mostly endocrine-related, and when the body experiences an endocrine disorder, hormone levels can also change, leading to otolithiasis.

3. Development issues.

Otolithiasis is related to developmental problems. Since humans are born, the bony labyrinth cyst has been developed. Only because the cartilage layer at the anterior edge of the vestibular has defects in the process of development and ossification, if it is not effective for a long time**, otolithiasis will slowly develop.

So be sure to do it in a timely manner**.

4. Ear diseases.

Ear diseases can also lead to otolithiasis. For example, conditions such as middle ear mastoid infection, vestibular neuritis, Meniere's disease, and sudden deafness with vertigo may be caused by otolithiasis or bilateral vestibular asymmetry. In addition, due to factors such as arteriosclerosis, high blood pressure, and diabetes, the blood supply to the inner ear is insufficient, and otolithiasis can also be caused.

1. Ear diseases, middle ear and mastoid infection, labyrinthitis, vestibular neuritis, sudden deafness, Meniere's disease in remission, etc. May be caused by oval cystic infarction or bilateral vestibular asymmetry.

Timely medical treatment, scientific**. 2. The sediment on the crest may be calcium carbonate crystals from otoliths, usually implanted in the inner ear balloon and elliptical balloon, which is aware of the spontaneous disintegration of the sand membrane and the labyrinth oscillation. Genetic factors: The direct ancestors and descendants of people with otosclerosis have the same disease, about 54% of people have a family history, some people think that it is autosomal dominant or recessive, and more than half of the cases can find abnormal genes.

3. Endocrine disorders are more common in adolescence and have a higher incidence in women. It accelerates the development of the disease during pregnancy, childbirth, and menopause, which is thought to be related to hormone levels. Developmental factors of labyrinth cysts Labyrinthine cysts develop at birth, but a defect during development and ossification remains in the introphyllous cartilage layer at the anterior border of the vestibular vestibule, called the anterior fissure.

The fissure contains bundles of fibrous connective tissue and cartilage tissue that persist or ossify into adulthood, creating otosclerosis lesions. Otosclerosis lesions seen clinically and in temporal bone pathology usually begin here.

It can only be said that there is this possibility, so if you have a disease, you still have to go to ** in time.

This still needs to be intervened in time.

Otolithiasis** is complex, partly** unknown, and partly related to nerve and ear diseases.

Essential**. Some patients** are unclear;

It can be secondary to head trauma, viral neuritis, vertebrobasilar artery circulation disorders, and some ear diseases such as Meniere's disease and otitis media;

Changes in calcium metabolism in the body may also be associated with the development of otolithiasis.