假性醛固酮减少症,pseudohypoaldosteronism
1)pseudohypoaldosteronism假性醛固酮减少症
1.Objective To improve the recognition of meconium ileus and pseudohypoaldosteronism type Ⅰ and to explore the relationship between neonatal meconium ileus and cystic fibrosis.目的提高对胎粪性肠梗阻和Ⅰ型假性醛固酮减少症的认识,探讨胎粪性肠梗阻与囊性纤维化的关系。
英文短句/例句

1.Meconium Ileus Combined with Pseudohypoaldosteronism Type Ⅰ in 1 Child胎粪性肠梗阻并Ⅰ型假性醛固酮减少症1例
2.secondary aldosteronism继发性醛固酮增多症
3.Licorice and glycyrrhizinic acid preparation-induced pseudohyperaldosteronism:prevention and treatment甘草及甘草酸制剂引起的假性醛固酮增多症及防治
4.glucocorticoid suppressible aldosteronism糖皮质类固醇可抑制性醛固酮症
5.Retrospective Analysis of 52 Patients with Primary Aldosteronism;原发性醛固酮增多症52例回顾性分析
6.PRIMARY ALDOSTERONISM(A CASE REPORT OF ADRENAL CORTICAL CARCINOMA)原发性醛固酮增多症(肾上腺皮质癌一例报告)
7.Study on Fuzzy Mathematical Diagnostic Cast of Primary Aldosteronism;原发性醛固酮增多症模糊数学诊断模型的研究
8.Analysis on Clinical Characteristics of 30 Patients with Primary Aldosteronism;原发性醛固酮增多症30例临床特点分析
9.Analysis on Clinical Characteristics of Hypertension in Patients with Primary Aldosteronism;原发性醛固酮增多症高血压临床特点分析
10.Clinical Analysis of Primary Aldosteronism;原发性醛固酮增多症的临床实践与分析
11.Diagnosis and surgical Treatment of primary Aldosteronism原发性醛固酮增多症的诊断与外科治疗
12.Retroperitoneal laparoscopic management of 29 patients with primary aldosteronism后腹腔镜手术治疗原发性醛固酮增多症29例
13.Association of Polymorphisms in CYP11B2 and CYP11B1 Genes with the Risk of Primary Aldosteronism醛固酮合酶和11-β羟化酶基因多态性与原发性醛固酮增多症发病风险的相关性研究
14.primary aldosteronism原发性醛甾酮增多症
15.Analysis of Clinical Data on the Inpatients with Primary Aldosteronism in West China Hospital from 1998 to 2006;华西医院1998年~2006年住院原发性醛固酮增多症患者的临床资料分析
16.The Clinical Analysis of 112 Cases with Primary Aldosteronism in Urumqi of Xinjiang;新疆乌鲁木齐地区原发性醛固酮增多症112例临床分析
17.Role of adrenal venous sampling in primary aldosteronism肾上腺静脉采血在原发性醛固酮增多症分型诊断中的价值
18.Treatment of primary aldosteronism with retroperitoneal laparoscopic surgery后腹腔镜手术治疗原发性醛固酮增多症133例临床体会
相关短句/例句

pseudohypoaldosteronism假醛固酮减少症
3)Pseudohypoaldosteronism Type 2假性醛固酮减少症Ⅱ型(PHAⅡ)
4)Pseudohypoaldosteronism type Ⅰ假性Ⅰ型低醛固酮血症
5)Psendohypoal dosteronism type Ⅱ假性低醛固酮血症Ⅱ型
6)pseudohypoaldosterism type IIⅡ型假性低醛固酮血症
延伸阅读

地塞米松可抑制性醛固酮增多症地塞米松可抑制性醛固酮增多症  〗【地塞米松可抑制性醛固酮增多症】(dexamethasone suppressible hyperaldosteronism,DSH)为常染色体遗传病。特点与原发性醛固酮增多症相同,但醛固酮的高分泌状态能迅速地完全被地塞米松所抑制,患儿症状好转,用其他皮质激素亦可使高血压缓解,但成人醛固酮虽被抑制而高血压可继续存在,变成顽固性高血压