Thyrotoxic Periodic Paralysis with Graves' Disease Leading to the Discovery of a Hidden Nonclassic 11β Hydroxylase Deficiency
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- Kim Jin Hwa
- Department of Endocrinology and Metabolism, Chosun University Hospital, Republic of Korea
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- Park Geon
- Department of Laboratory Medicine, Chosun University Hospital, Republic of Korea
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- Kim Sang Yong
- Department of Endocrinology and Metabolism, Chosun University Hospital, Republic of Korea
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- Bae Hak Yeon
- Department of Endocrinology and Metabolism, Chosun University Hospital, Republic of Korea
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抄録
11β hydroxylase deficiency (OHD) is one of the main causes of congenital adrenal hyperplasia. There have been only a few reported cases of nonclassic 11β OHD, a milder form of the disease. It is difficult to detect occult nonclassic 11β OHD because patients present with no or mild symptoms. We herein present a case of thyrotoxic periodic paralysis (TPP) with Graves' disease leading to the discovery of a hidden nonclassic 11β OHD. In this case, increased levels of thyroid hormone seem to have induced symptoms of occult nonclassic 11β OHD and aggravated TPP.<br>
収録刊行物
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- Internal Medicine
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Internal Medicine 52 (1), 85-88, 2013
一般社団法人 日本内科学会