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Two Case of Primary Aldosteronism Induced by Aldosterone Producing Adrenal Adenoma in a Family

Jang YR, Kim SH, Eom YS, Lee KY

Primary aldosteronism, is defined as a group of disorders characterized by the excess of aldosteron, with suppressed rennin activity, resulting in hypertension and hypokalemia. In most cases, primary aldosteronism is...
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A Case of Licorice Induced Hypokalemic Paralysis with Rhabdomyolysis

Hong HI, Han KH, Hwang JW, Kim YD, Shim MS, Kim JY

  • KMID: 2331200
  • J Korean Soc Endocrinol.
  • 2005 Apr;20(2):179-182.
Prolonged ingestion of licorice can cause hypermineralocorticoidism, with sodium retention, potassium loss and hypertension. Nevertheless, its initial presentation with a very severe degree of hypokalemic paralysis and rhabdomyolysis are exceedingly...
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ANCA-related crescentic glomerulonephritis in a patient with systemic sclerosis

Kwon JS, Shin YK, Kwak JH, Park SH, Kim SK, Choe JY

  • KMID: 2081675
  • Korean J Med.
  • 2009 Apr;76(Suppl 1):S154-S157.
The renal manifestations of systemic sclerosis include proteinuria, hypertension, azotemia, and renal crisis. Two types of scleroderma renal crisis (SRC) are recognized. Typical SRC is a syndrome consisting of acute-onset...
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A Case of Male Pseudohermaphroditism due to 17alpha-Hydroxylase Deficiency

Park KA, Chung YK, Lee JR, Choi YM, Lee GH, Kim HS, Jee BC, Ku SY, Suh CS, Kim SH, Kim JG, Moon SY, Kim SY

  • KMID: 1830752
  • Korean J Fertil Steril.
  • 2006 Jun;33(2):133-138.
Female phenotype of a 46,XY male may originates from male pseudohermaphroditism due to 17alpha-hydroxylase deficiency. Lack of cortisol increases adrenocorticotropic hormone (ACTH) and mineralocorticoid production, leading to low renin hypertention...
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1 Case of Primary Aldosteronism Caused by Adrenal Hyperplasia

Park SH, Choi SB, Kim CS

Primary aldosteronism is a disease that the stimulus for the excessive aldosterone production residues within the adrenal gland. It was first described by conn in 1955. And many cases were reported...
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