Literature DB >> 23291679

Thyrotoxic periodic paralysis with Graves' disease leading to the discovery of a hidden nonclassic 11β hydroxylase deficiency.

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.

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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


  3 in total

1.  Roux-en-Y gastric bypass in the treatment of non-classic congenital adrenal hyperplasia due to 11-hydroxylase deficiency.

Authors:  Amir Kalani; Nithin Thomas; Alan Sacerdote; Gül Bahtiyar
Journal:  BMJ Case Rep       Date:  2013-03-18

2.  Congenital lipoid adrenal hyperplasia with Graves' disease: A case report.

Authors:  Yan-Jun Wang; Cong Liu; Chuan Xing; Le Zhang; Wan-Feng Xu; Hai-Ying Wang; Fu-Tao Wang
Journal:  World J Clin Cases       Date:  2022-09-16       Impact factor: 1.534

3.  Graves' Thyrotoxicosis Leading to Adrenal Decompensation and Hyperandrogenemia in a Pediatric Patient with Salt-Wasting Congenital Adrenal Hyperplasia.

Authors:  Meghan E Fredette; Lisa Swartz Topor
Journal:  Case Rep Endocrinol       Date:  2018-11-22
  3 in total

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