グルココルチコイド奏効性アルドステロン症
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- 1. 家族性アルドステロン症familial hyperaldosteronism [show details]
…early cerebrovascular complications in patients with GRA have been confirmed in a review from the international registry for GRA . Among patients with GRA, 18 percent had a cerebrovascular complication, 70 …
- 2. まれな先天性副腎過形成uncommon congenital adrenal hyperplasias [show details]
…CYP11B1 and CYP11B2 genes , which is reminiscent of the genetic event leading to glucocorticoid-remediable aldosteronism (GRA). The goals of therapy in children with 11OHD are to reduce mineralocorticoid…
- 3. 原発性アルドステロン症の診断diagnosis of primary aldosteronism [show details]
…rule in patients with the rare genetic disorder glucocorticoid-remediable aldosteronism (GRA). There are, however, important physiologic differences between GRA and other forms of hyperaldosteronism that could …
- 4. 原発性アルドステロン症の治療treatment of primary aldosteronism [show details]
…aldosteronism. Other causes are reviewed elsewhere: Familial hyperaldosteronism type I (glucocorticoid-remediable aldosteronism [GRA]), type II (the familial occurrence of APA or bilateral IHA or both), type III …
- 5. 原発性アルドステロン症の病態生理および臨床的特徴pathophysiology and clinical features of primary aldosteronism [show details]
…patients is similar to those with APAs . Familial hyperaldosteronism (FH) type I (glucocorticoid-remediable aldosteronism [GRA]), type II (the familial occurrence of APA or bilateral IHA or both), type III…
English Journal
- Family hyperaldosteronism type I: a clinical case and review of literature.
- Chikladze NM, Favorova OO, Chazova IE.
- Terapevticheskii arkhiv. 2018 Sep;90(9)115-122.
- Family hyperaldosteronism type I (glucocorticoids-remediable hyperaldosteronism) is a rare form of symptomatic arterial hypertension (AH), which often leads to the development of cerebrovascular complications. The disease is caused by the formation of the chimeric gene CYP11B2/CYP11B1. Expression
- PMID 30701745
- Glucocorticoid-remediable aldosteronism in a young adult with a family history of Conn's syndrome.
- Methe H, Pehlivanli S.
- Clinical case reports. 2018 02;6(2)416-419.
- Glucocorticoid-remediable aldosteronism is a hereditary form of primary hyperaldosteronism and the most common monogenic cause of hypertension. We present the case of a 24-year-old man with a family history of Conn's syndrome. Yet, in the index patient, classical characteristics of mineralocorticoid
- PMID 29445488
- DIAGNOSIS OF ENDOCRINE DISEASE: 18-Oxocortisol and 18-hydroxycortisol: is there clinical utility of these steroids?
- Lenders JWM, Williams TA, Reincke M, Gomez-Sanchez CE.
- European journal of endocrinology. 2018 Jan;178(1)R1-R9.
- Since the early 1980s 18-hydroxycortisol and 18-oxocortisol have attracted attention when it was shown that the urinary excretion of these hybrid steroids was increased in primary aldosteronism. The development and more widespread use of specific assays has improved the understanding of their role i
- PMID 28904009
Japanese Journal
- Polyuric-polydipsic syndrome in a pediatric case of non-glucocorticoid remediable familial hyperaldosteronism
- MUSSA Alessandro,CAMILLA Roberta,MONTICONE Silvia,PORTA Francesco,TESSARIS Daniele,VERNA Francesca,MULATERO Paolo,EINAUDI Silvia
- Endocrine journal 59(6), 497-502, 2012-06-01
- … Familial hyperaldosteronism (FH) encompasses 3 types of autosomal dominant hyperaldosteronisms leading to inheritable hypertension. … FH type II (FH-II), undistinguishable from sporadic hyperaldosteronism, represents the most frequent cause of inheritable hypertension and is believed to only manifest in adults. … FH type I was ruled out by glucocorticoid suppression test, PCR test for <i>CYP11B1/CYP11B2</i> …
- NAID 10030816811
- Genetic Alterations in Patients with Primary Aldosteronism.
- TAKEDA Yoshiyu
- Hypertension Research 24(5), 469-474, 2001
- … The most common clinical subtypes of primary aldosteronism are aldosterone-producing adrenocortical adenoma (APA) and bilateral adrenal cortical hyperplasia (idiopathic hyperaldosteronism, or IHA). … gene, which is a candidate gene for glucocorticoid-remediable hyperaldosteronism, was not found in either the DNA from aldosteronoma or in the genomic DNA from patients with APA or IHA. …
- NAID 130004436919
- キメラ遺伝子が証明されたグルココルチコイド反応性アルドステロン症の母子例
- 上牧 務,佐藤 清二,安蔵 慎,室谷 浩二,菅谷 憲夫,本間 桂子,千葉 仁志,松尾 宣武
- 日本先天代謝異常学会雑誌 11(2), 110, 1995-10-05
- NAID 10018923069
Related Links
- 1. Endocrinol Metab Clin North Am. 2011 Jun;40(2):333-41, viii. doi: 10.1016/j.ecl.2011.01.012. Glucocorticoid-remediable aldosteronism. Halperin F(1), Dluhy RG. Author information: (1)Division of Endocrinology, Diabetes ...
- Glucocorticoid-remediable aldosteronism (GRA), alternatively called dexamethasone-suppressible hyperaldosteronism (DSH) or familial hyperaldosteronism type I, a mineralocorticoid-excess state characterized by low PRA, is now ...
- Glucocorticoid-remediable aldosteronism is one of three types of familial hyperaldosteronism. Aldosterone is a hormone manufactured by the adrenal glands which helps the body retain water and sodium and excrete ...
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- 英
- glucocorticoid remediable hyperaldosteronism GCRHA
- 関
- 原発性アルドステロン症
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糖質コルチコイド
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高アルドステロン症
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