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Autoimmune polyendocrine syndrome type 2 : ウィキペディア英語版
Autoimmune polyendocrine syndrome type 2

Autoimmune polyendocrine syndrome type 2, a form of autoimmune polyendocrine syndrome also known as Schmidt's syndrome, or APS-II, is the most common form of the polyglandular failure syndromes. It is heterogeneous and has not been linked to one gene. Rather, patients are at a higher risk when they carry a particular human leukocyte antigen genotype (HLA-DQ2, HLA-DQ8 and HLA-DR4). APS-II affects women to a greater degree than men (75% of cases occur in women).〔
Features of this syndrome are:
* Addison's disease
* Primary hypothyroidism
* Graves' disease
* Pernicious anaemia
* Primary hypogonadism (less common)
* Diabetes mellitus (type 1)
* Vitiligo (less common)
* Coeliac disease
* Myasthenia gravis
==Symptoms==
Symptoms of Addison's disease and Hashimoto's thyroiditis include:
* Dry hair
* Nausea
* Abdominal Pain
* Frequent urination
* Vomiting
* Weight and muscle loss
* Salt cravings / salt wasting
* Anorexia and cachexia
* High pulse / weakened heart
* Low blood pressure
* Weakness
* Hypoglycemia
* Numbness in extremities
* Migraines / dysparunia
* Poor immune system response
Some researchers favour splitting this syndrome into three distinct syndromes (numbering 2, 3 and 4), but evidence for these distinct combinations is not convincing.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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