自免疫多腺综合征II:一个病例报告
Olfat Awad1, Hadil Basma2, Rim Masri2
1Department of Nephrology, Lebanese University Faculty of Medical Sciences, Beirut, LBN.
Cureus
|February 16, 2024
概括
自免疫多腺综合征II (APS-II),或施密特综合征,涉及多种自身免疫性疾病. 对于患有现有的自身免疫性疾病的患者来说,早期诊断至关重要,以确定潜在的上腺功能不足.
科学领域:
- 内分泌学 在内分泌学.
- 免疫学 免疫学 免疫学
- 遗传学 遗传学 是一个
背景情况:
- 自免疫多腺综合征II (APS-II),也称为施密特综合征,是一种罕见的内分泌疾病.
- 它的特征是自身免疫性多性腺发病 - - 候选症 - - 皮肤外 (APECED) 和自身免疫性甲状腺疾病或1型糖尿病 (T1DM).
- APS-II是由遗传和非遗传因素的结合导致的.
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