What Is Cushing’s Syndrome?
Endocrinologie Infantile

What Is Cushing’s Syndrome?

    What Is Cushing’s Syndrome?


    Cushing’s disease is a rare condition that causes high levels of cortisol in the body. It can be caused by an adrenal tumor or pituitary adenoma.

    Cushing’s syndrome occurs when there is too much cortisol circulating in the blood. The excess cortisol affects many parts of the body, causing symptoms like weight gain, fatigue, and muscle weakness.


    Learn more about this condition and how it affects people

    Cushing’ s syndrome is a rare endocrine disorder that results in increased production of cortisol. This hormone is produced by the adrenal glands and helps regulate metabolism. In some cases, the cause of the disorder is an adrenal gland tumor called an adrenocortical carcinoma (ACC). Other times, the cause is a benign growth called a pituitary adenomas.


    What Is Cushing‘s Disease?

    Cushing’S disease is a rare endocrine disease that occurs when there is too much cortisol in the body. Cortisol is a steroid hormone made by the adrenal glands. It regulates blood sugar and other functions.


    Symptoms of Cushing’s Disease

    Cushing’ s disease is characterized by symptoms such as weight gain, fatigue, muscle weakness, and low energy. Other signs and symptoms include acne, hair loss, increased appetite, and changes in mood.


    Causes of Cushing’S Disease

    Cushing’S disease is a rare endocrine disorder that occurs when there is too much cortisol in the body. This excess cortisol comes from either an adrenal gland tumor or a pituitary adenomas.


    Diagnosis of Cushing’ S Disease

    If you think you might have Cushing’s syndrome, talk with your doctor right away. He or she will perform tests to determine whether you do indeed have the condition. These tests include blood tests, urine tests, and imaging studies such as CT scans and MRI scans.

    The content of the page is for informational purposes only, please consult your doctor for diagnosis and treatment.

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    Approved by on 01.09.2022

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