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迪乔治综合征中的格雷夫斯病:病例报告及与22q11.2缺失相关的内分泌自身免疫性综述

Graves' disease in DiGeorge syndrome: patient report with a review of endocrine autoimmunity associated with 22q11.2 deletion.

作者信息

Brown J J, Datta V, Browning M J, Swift P G F

机构信息

Royal Children 's Hospital, Parkville, Victoria, Australia.

出版信息

J Pediatr Endocrinol Metab. 2004 Nov;17(11):1575-9. doi: 10.1515/jpem.2004.17.11.1575.

Abstract

DiGeorge syndrome, which falls within a wider phenotypic spectrum associated with deletions of 22q11.2, is associated with a number of endocrine disorders. These include hypoparathyroidism, hypothyroidism and growth hormone deficiency. We report an unusual case of autoimmune hyperthyroidism (Graves' disease) presenting in a 3 year-old male with DiGeorge syndrome. The development of endocrine specific autoimmune disease in a syndrome associated with immune deficiency and the spectrum of endocrine autoimmunity associated with deletions of 22q11.2 are described. Paediatricians and patients with 22q11.2 deletions should be particularly aware of the risks of developing disorders of thyroid function.

摘要

迪乔治综合征属于与22q11.2缺失相关的更广泛表型谱,与多种内分泌疾病有关。这些疾病包括甲状旁腺功能减退、甲状腺功能减退和生长激素缺乏。我们报告了一例罕见病例,一名患有迪乔治综合征的3岁男性出现自身免疫性甲状腺功能亢进(格雷夫斯病)。本文描述了在一种与免疫缺陷相关的综合征中发生内分泌特异性自身免疫性疾病以及与22q11.2缺失相关的内分泌自身免疫谱。儿科医生和患有22q11.2缺失的患者应特别注意发生甲状腺功能障碍的风险。

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