Do I have type 2 polyglandular autoimmune syndrome?

Do I have type 2 polyglandular autoimmune syndrome?

PAS-2 is diagnosed when at least 2 out of 3 of the following are present: primary adrenal insufficiency (Addison disease), autoimmune thyroid disease-causing Grave’s disease or hypothyroidism, and type 1 diabetes mellitus (T1DM).

What is Polyendocrine syndrome type II?

Autoimmune polyendocrine syndrome type II, also known as Schmidt syndrome, is a rare autoimmune disorder in which there is a steep drop in production of several essential hormones by the glands that secrete these hormones.

What is Polyglandular autoimmune syndrome?

Autoimmune polyglandular syndrome type 1 (APS-1) is a rare and complex recessively inherited disorder of immune-cell dysfunction with multiple autoimmunities. It presents as a group of symptoms including potentially life-threatening endocrine gland and gastrointestinal dysfunctions.

What is a Polyendocrine disorder?

Autoimmune polyendocrine syndrome is a rare, inherited disease in which the immune system mistakenly attacks many of the body’s tissues and organs. The mucous membranes and adrenal and parathyroid glands are commonly affected, though other tissues and organs may become involved as well.

Is Addison disease fatal?

People with Addison’s disease must be constantly aware of the risk of a sudden worsening of symptoms, called an adrenal crisis. This can happen when the levels of cortisol in your body fall significantly. An adrenal crisis is a medical emergency. If left untreated, it can be fatal.

How does autoimmune Polyglandular syndrome affect the immune system?

What causes Polyglandular syndrome?

While the cause of polyglandular autoimmune syndrome type 2 is not fully understood, it usually results from an autoimmune reaction, probably triggered by a virus or other environmental antigen. There is some evidence of an association between diabetes or hypothyroidism and congenital rubella infection.