首页> 外文期刊>The American Journal of the Medical Sciences >Autoimmune polyendocrine syndrome with atrial septal defect.
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Autoimmune polyendocrine syndrome with atrial septal defect.

机译:房间隔缺损的自身免疫性多内分泌综合征。

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摘要

Atrial septal defect is frequently reported with genetic syndromes. But, to the best of our knowledge, it has not been reported with autoimmune polyendocrine syndrome. Here, the case of a 44-year-old-woman with concomitant involvement of the salivary gland, thyroid, intestines, and, possibly endocrine pancreas, diagnosed with autoimmune polyendocrine syndrome type II, is reported with accompanying atrial septal defect. Celiac disease, Hashimoto thyroiditis, and Sjogren syndrome were symptomatic and laboratory confirmed diagnosis; anti-glutamic acid decarboxylase antibody was positive but asymptomatic for type-1 diabetes. She was known to have sinus venosus type atrial septal defect diagnosed at 38 years old, when she had tiredness and chest pain.
机译:房间隔缺损常被报道为遗传综合征。但是,据我们所知,尚未报道自身免疫性多内分泌综合征。在此,据报道,一名44岁的女性伴有唾液腺,甲状腺,肠道以及可能的内分泌胰腺受累,被诊断出患有自身免疫性多内分泌综合征II型,并伴有房间隔缺损。有症状的有腹腔疾病,桥本甲状腺炎和干燥综合征,并经实验室确认诊断。抗谷氨酸脱羧酶抗体呈阳性,但对1型糖尿病无症状。已知她在38岁时患有疲倦和胸痛,诊断为窦性静脉窦型房间隔缺损。

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