- Secondary Hypertension Caused by Endocrine Disorders Except Primary Aldosteronism and Pheochromocytoma
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Kim DS
- KMID: 2264288
- Korean J Med.
- 2012 Apr;82(4):411-416.
Secondary hypertension can account for 15% of hypertension cases. The causes of secondary hypertension mostly come from renal diseases, such as renal parenchymal or renovascular disease, and endocrine diseases. The... -
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- Corticosteroids Treatment in Spinal Cord and Neuromuscular Disorders
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Na SJ
- KMID: 2405761
- J Neurocrit Care.
- 2017 Dec;10(2):76-85.
- doi: 10.18700/jnc.170032
Corticosteroids are a class of steroid hormones that are produced in the adrenal cortex of the vertebrates, as well as the synthetic analogs of these hormones that are synthesized in... -
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- Molecular Mechanisms of Primary Aldosteronism
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Tevosian S, Fox SC, Ghayee HK
- KMID: 2466254
- Endocrinol Metab.
- 2019 Dec;34(4):355-366.
- doi: 10.3803/EnM.2019.34.4.355
Primary aldosteronism (PA) results from excess production of mineralocorticoid hormone aldosterone by the adrenal cortex. It is normally caused either by unilateral aldosterone-producing adenoma (APA) or by bilateral aldosterone excess... -
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- Congenital Adrenal Agenesis Presented with Adrenal Insufficiency
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Park HK, Shim EJ, Lee KS, Hwang IT
- KMID: 1434744
- Ann Pediatr Endocrinol Metab.
- 2012 Mar;17(1):53-56.
- doi: 10.6065/apem.2012.17.1.53
We report a very rare case of congenital adrenal agenesis presented with adrenal insufficiency in a 4-day-old female newborn. She was admitted with darkish skin color and seizure. Her external... -
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- A case of 17 alpha-hydroxylase deficiency
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Kim SM, Rhee JH
- KMID: 1879368
- Clin Exp Reprod Med.
- 2015 Jun;42(2):72-76.
- doi: 10.5653/cerm.2015.42.2.72
17alpha-hydroxylase and 17,20-lyase are enzymes encoded by the CYP17A1 gene and are required for the synthesis of sex steroids and cortisol. In 17alpha-hydroxylase deficiency, there are low blood levels of... -
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- Pseudohypoaldosteronism Type 1
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Cheong HI
- KMID: 1811001
- J Genet Med.
- 2013 Dec;10(2):81-87.
- doi: 10.5734/JGM.2013.10.2.81
Pseudohypoaldosteronism (PHA), a rare syndrome of systemic or renal mineralocorticoid resistance, is clinically characterized by hyperkalemia, metabolic acidosis, and elevated plasma aldosterone levels with either renal salt wasting or hypertension.... -
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- A Case of Glycyrrhizin (Licorice)-induced Hypokalemic Myopathy
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Kim BJ, Hong YH, Sung JJ, Park KS, Hyun CL, Choe G, Park SH, Lee KW
- KMID: 2343238
- J Korean Neurol Assoc.
- 2006 Aug;24(4):389-391.
Glycyrrhizin, the main ingredient of licorice, may evoke severe hypokalemia and muscle paralysis by its mineralocorticoid effects. We present a 78-year-old man who developed subacute flaccid quadriparesis with a high... -
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- Hypertensive Hypokalemic Disorders
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Choi KB
- KMID: 2134803
- Electrolyte Blood Press.
- 2007 Jun;5(1):34-41.
- doi: 10.5049/EBP.2007.5.1.34
Hypokalemia is a common clinical problem. The kidney is responsible for long term potassium homoeostasis, as well as the serum potassium concentration. The main nephron site where K secretion is... -
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- Effect of Mineralocorticoid on Serum Potassium Regulation and Urine Ammonium Excretion in Chronic Renal Patients
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Lee SJ, Jeon US, Chin HJ, Huh WS, Cho YS, Kim KS, Joo KW, Han JS, Kim SG, Lee JS
- KMID: 2079083
- Korean J Nephrol.
- 2000 Mar;19(2):278-284.
Mineralocorticoids influences on acid-base homeostasis by the regulation of urine acidification. But its mechanism of acion is not well known in human. This study compared the acid-base status and the... -
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- Clinical Features of Congenital Adrenal Insufficiency Including Growth Patterns and Significance of ACTH Stimulation Test
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Koh JW, Kim GH, Yoo HW, Yu J
- KMID: 1777664
- J Korean Med Sci.
- 2013 Nov;28(11):1650-1656.
- doi: 10.3346/jkms.2013.28.11.1650
Congenital adrenal insufficiency is caused by specific genetic mutations. Early suspicion and definite diagnosis are crucial because the disease can precipitate a life-threatening hypovolemic shock without prompt treatment. This study... -
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