A Rare Case of Hypertension in a Young (Fe)male.
作者信息
Golla Anvesh, Raju Sreebhushan, Prasad Krishna
机构信息
Department of Nephrology, Nizams Institute of Medical Sciences, Hyderabad, Telangana, India.
出版信息
Indian J Nephrol. 2020 Mar-Apr;30(2):133-135. doi: 10.4103/ijn.IJN_446_17. Epub 2020 Feb 11.
Abstract
摘要
相似文献
1
A Rare Case of Hypertension in a Young (Fe)male.一名年轻（女）性高血压罕见病例。
Indian J Nephrol. 2020 Mar-Apr;30(2):133-135. doi: 10.4103/ijn.IJN_446_17. Epub 2020 Feb 11.
2
Failed extubation after cardiac surgery in young children: Prevalence, pathogenesis, and risk factors.小儿心脏手术后拔管失败：发生率、发病机制及危险因素
Pediatr Crit Care Med. 2002 Apr;3(2):148-152. doi: 10.1097/00130478-200204000-00011.
3
The relation between ACE D/I and CYP11B2 C-344T polymorphisms and parameters of arterial stiffness in the context of renal sodium handling.在肾脏钠处理背景下，ACE D/I和CYP11B2 C-344T基因多态性与动脉僵硬度参数之间的关系。
Blood Press. 2015;24(5):306-16. doi: 10.3109/08037051.2015.1070476.
4
Combination of renin-angiotensin system polymorphisms is associated with altered renal sodium handling and hypertension.肾素 - 血管紧张素系统基因多态性的组合与肾钠处理改变及高血压相关。
Hypertension. 2004 Mar;43(3):598-602. doi: 10.1161/01.HYP.0000117985.57001.b3. Epub 2004 Feb 16.
5
Resistant Hypertension due to Fibromuscular Dysplasia in a Young Male: A Rare Case Report.一名年轻男性因纤维肌发育不良导致的难治性高血压：一例罕见病例报告
J Clin Diagn Res. 2016 Jun;10(6):OD08-9. doi: 10.7860/JCDR/2016/20069.7938. Epub 2016 Jun 1.
6
A rare case of juvenile hypertension: coexistence of type 2 multiple endocrine neoplasia -related bilateral pheochromocytoma and reninoma in a young patient with ACE gene polymorphism.青少年高血压罕见病例：一名存在ACE基因多态性的年轻患者中，2型多发性内分泌肿瘤相关双侧嗜铬细胞瘤与肾素瘤并存。
BMC Endocr Disord. 2015 Jun 18;15:30. doi: 10.1186/s12902-015-0022-5.
7
Enhanced sodium retention after acute nitric oxide blockade in mildly sodium loaded patients with essential hypertension.轻度钠负荷原发性高血压患者急性一氧化氮阻断后钠潴留增强。
Am J Hypertens. 2007 Mar;20(3):287-95. doi: 10.1016/j.amjhyper.2006.09.008.
8
Incidence, risk factors and short-term mortality of stroke in Vittoria, southern Italy.意大利南部维多利亚市中风的发病率、危险因素及短期死亡率
Neurol Sci. 2002 Apr;23(1):15-21. doi: 10.1007/s100720200018.
9
Uhl's Anomaly: A Rare Case of Portal Hypertension.乌尔氏异常：门静脉高压症的罕见病例。
Heart Views. 2016 Oct-Dec;17(4):142-145. doi: 10.4103/1995-705X.201779.
10
Pheochromocytoma as a rare cause of hypertension in a 46 X, i(X)(q10) turner syndrome: a case report and literature review.46,X,i(X)(q10)特纳综合征中嗜铬细胞瘤作为高血压的罕见病因：一例报告及文献综述
BMC Endocr Disord. 2018 May 10;18(1):27. doi: 10.1186/s12902-018-0253-3.
引用本文的文献
1
11β Hydroxylase Deficiency in a Child with Hypothyroidism: A Case Report.11β 羟化酶缺乏症合并甲状腺功能减退症患儿 1 例报告
JNMA J Nepal Med Assoc. 2023 Dec 1;61(268):956-957. doi: 10.31729/jnma.8378.
本文引用的文献
1
The next 150 years of congenital adrenal hyperplasia.先天性肾上腺皮质增生症的未来150年
J Steroid Biochem Mol Biol. 2015 Sep;153:63-71. doi: 10.1016/j.jsbmb.2015.05.013. Epub 2015 Jun 3.
2
Disorders of sex development: clinically relevant genes involved in gonadal differentiation.性发育障碍：性腺分化中涉及的临床相关基因
Discov Med. 2012 Nov;14(78):301-9.
3
17α-hydroxlyase/17, 20-lyase deficiency in three siblings with primary amenorrhea and absence of secondary sexual development.三名原发性闭经且无第二性征发育的同胞姐妹中存在17α-羟化酶/17,20-裂解酶缺乏症。
J Pediatr Adolesc Gynecol. 2012 Oct;25(5):e103-5. doi: 10.1016/j.jpag.2012.05.008. Epub 2012 Jul 27.
4
Congenital adrenal hyperplasia: a rare cause of renal failure and a successful renal transplantation.先天性肾上腺增生症：肾衰竭的罕见病因及成功的肾移植病例
Clin Nephrol. 2012 Aug;78(2):145-8. doi: 10.5414/cn107032.
5
Diagnosis of diseases of steroid hormone production, metabolism and action.类固醇激素产生、代谢及作用相关疾病的诊断
J Clin Res Pediatr Endocrinol. 2009;1(5):209-26. doi: 10.4274/jcrpe.v1i5.209. Epub 2009 Aug 2.
6
Congenital adrenal hyperplasia.先天性肾上腺增生症
N Engl J Med. 2003 Aug 21;349(8):776-88. doi: 10.1056/NEJMra021561.
7
17-hydroxylation deficiency in man.人类17-羟化酶缺乏症
J Clin Invest. 1966 Dec;45(12):1946-54. doi: 10.1172/JCI105499.
8
Congenital adrenal hyperplasias.先天性肾上腺增生症
Endocrinol Metab Clin North Am. 1991 Dec;20(4):721-49.
Zotero 插件