| Literature DB >> 23291679 |
Jin Hwa Kim1, Geon Park, Sang Yong Kim, Hak Yeon Bae.
Abstract
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.Entities:
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Year: 2013 PMID: 23291679 DOI: 10.2169/internalmedicine.52.8032
Source DB: PubMed Journal: Intern Med ISSN: 0918-2918 Impact factor: 1.271