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结节性硬化症中的甲状腺发育不全与发育异常假说

Thyroid dysgenesis and the dysplasia hypothesis in tuberous sclerosis.

作者信息

Bereket A, Wilson T A

机构信息

Department of Pediatrics, State University of New York, Stony Brook.

出版信息

Am J Med Genet. 1993 Sep 1;47(3):417-9. doi: 10.1002/ajmg.1320470324.

Abstract

Thyroid dysfunction is rare in tuberous sclerosis, although papillary adenomas (hamartomas) of the thyroid gland have been reported in a few autopsy cases. We describe a child with tuberous sclerosis and primary congenital hypothyroidism secondary to a dysgenetic thyroid gland. To our knowledge, this association has not been reported previously. Although the association of these two disorders in one patient may be merely coincidence, we speculate that the dysgenetic thyroid gland in this patient may represent a "hamartia" as a consequence of the tuberous sclerosis gene.

摘要

结节性硬化症患者甲状腺功能障碍较为罕见,尽管在少数尸检病例中曾报告过甲状腺乳头状腺瘤(错构瘤)。我们描述了一名患有结节性硬化症且因甲状腺发育异常导致原发性先天性甲状腺功能减退的儿童。据我们所知,此前尚未有这种关联的报道。虽然这两种病症在一名患者身上同时出现可能仅仅是巧合,但我们推测该患者甲状腺发育异常可能是结节性硬化症基因导致的一种“发育异常”。

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