Male pseudohermaphroditism presented with sudden cardiac arrest

Jaemin Shim; Hye Jin Hwang; Hui Nam Pak; Moon Hyoung Lee; Boyoung Joung

doi:10.3349/ymj.2012.53.3.658

Male pseudohermaphroditism presented with sudden cardiac arrest

Jaemin Shim, Hye Jin Hwang, Hui Nam Pak, Moon Hyoung Lee, Boyoung Joung

Department of Internal Medicine

Research output: Contribution to journal › Article › peer-review

Abstract

Torsades de Pointes is a life-threatening arrhythmia associated with a number of causes, but is very rare among endocrinologic disorders. We report a case of male pseudohermaphroditism with hyperaldosteronism due to a 17α-hydroxylase deficiency presented with sudden cardiac arrest.

Original language	English
Pages (from-to)	658-661
Number of pages	4
Journal	Yonsei medical journal
Volume	53
Issue number	3
DOIs	https://doi.org/10.3349/ymj.2012.53.3.658
Publication status	Published - 2012 May

All Science Journal Classification (ASJC) codes

Medicine(all)

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10.3349/ymj.2012.53.3.658

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title = "Male pseudohermaphroditism presented with sudden cardiac arrest",

abstract = "Torsades de Pointes is a life-threatening arrhythmia associated with a number of causes, but is very rare among endocrinologic disorders. We report a case of male pseudohermaphroditism with hyperaldosteronism due to a 17α-hydroxylase deficiency presented with sudden cardiac arrest.",

author = "Jaemin Shim and Hwang, {Hye Jin} and Pak, {Hui Nam} and Lee, {Moon Hyoung} and Boyoung Joung",

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AU - Pak, Hui Nam

AU - Lee, Moon Hyoung

AU - Joung, Boyoung

PY - 2012/5

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N2 - Torsades de Pointes is a life-threatening arrhythmia associated with a number of causes, but is very rare among endocrinologic disorders. We report a case of male pseudohermaphroditism with hyperaldosteronism due to a 17α-hydroxylase deficiency presented with sudden cardiac arrest.

AB - Torsades de Pointes is a life-threatening arrhythmia associated with a number of causes, but is very rare among endocrinologic disorders. We report a case of male pseudohermaphroditism with hyperaldosteronism due to a 17α-hydroxylase deficiency presented with sudden cardiac arrest.

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Male pseudohermaphroditism presented with sudden cardiac arrest

Abstract

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