[1]
|
Konrad M, Nijenhuis T, Ariceta G, et al. Diagnosis and management of Bartter syndrome: executive summary of the consensus and recommendations from the European Rare Kidney Disease Reference Network Working Group for Tubular Disorders[J]. Kidney Int, 2021, 99: 324-335. doi: 10.1016/j.kint.2020.10.035 |
[2]
|
Graham AJ, Gelfand G, McFadden SD, et al. Levels of evidence and grades of recommendations in general thoracic surgery[J]. Can J Surg, 2004, 47: 461-465. |
[3]
|
王建祥, 张奉春, 刘晓清, 等. 中国成人血小板减少症诊疗专家共识[J]. 中华内科杂志, 2020, 59: 498-510. doi: 10.3760/cma.j.cn112138-20200424-00419 |
[4]
|
Jones J, Hunter D. Consensus methods for medical and health services research[J]. BMJ, 1995, 311: 376-380. doi: 10.1136/bmj.311.7001.376 |
[5]
|
Bamgbola OF, Ahmed Y. Differential diagnosis of perinatal Bartter, Bartter and Gitelman syndromes[J]. Clin Kidney J, 2021, 14: 36-48. doi: 10.1093/ckj/sfaa172 |
[6]
|
Seys E, Andrini O, Keck M, et al. Clinical and genetic spectrum of Bartter syndrome type 3[J]. J Am Soc Nephrol, 2017, 28: 2540-2552. doi: 10.1681/ASN.2016101057 |
[7]
|
Legrand A, Treard C, Roncelin I, et al. Prevalence of novel MAGED2 mutations in antenatal Bartter syndrome[J]. Clin J Am Soc Nephrol, 2018, 13: 242-250. doi: 10.2215/CJN.05670517 |
[8]
|
Lee HS, Cheong HI, Ki CS. A case of antenatal Bartter syndrome with sensorineural deafness[J]. J Pediatr Endocrinol Metab, 2010, 23: 1077-1081. |
[9]
|
Finer G, Shalev H, Birk OS, et al. Transient neonatal hyperkalemia in the antenatal (ROMK defective) Bartter syndrome[J]. J Pediatr, 2003, 142: 318-323. doi: 10.1067/mpd.2003.100 |
[10]
|
Birkenhager R, Otto E, Schurmann MJ, et al. Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure[J]. Nat Genet, 2001, 29: 310-314. doi: 10.1038/ng752 |
[11]
|
Shalev H, Ohali M, Kachko L, et al. The neonatal variant of Bartter syndrome and deafness: preservation of renal function[J]. Pediatrics, 2003, 112: 628-633. doi: 10.1542/peds.112.3.628 |
[12]
|
Takemori S, Tanigaki S, Nozu K, et al. Prenatal diagnosis of MAGED2 gene mutation causing transient antenatal Bartter syndrome[J]. Eur J Med Genet, 2021, 64: 104308. doi: 10.1016/j.ejmg.2021.104308 |
[13]
|
Laghmani K, Beck BB, Yang SS, et al. Polyhydramnios, transient antenatal Bartter's syndrome, and MAGED2 mutations[J]. N Engl J Med, 2016, 374: 1853-1863. doi: 10.1056/NEJMoa1507629 |
[14]
|
韩玥, 郎艳华, 林毅, 等. 42例3型巴特综合征CLCNKB基因变异分析和基因型/表型研究[J]. 中华肾脏病杂志, 2019, 35: 499-506. doi: 10.3760/cma.j.issn.1001-7097.2019.07.004 |
[15]
|
London S, Levine MA, Li D, et al. Hypocalcemia as the initial presentation of type 2 Bartter syndrome: a family report[J]. J Clin Endocrinol Metab, 2022, 107: 1679-1688. doi: 10.1210/clinem/dgac130 |
[16]
|
Brum S, Rueff J, Santos JR, et al. Unusual adult-onset manifestation of an attenuated Bartter's syndrome type Ⅳ renal phenotype caused by a mutation in BSND[J]. Nephrol Dial Transplant, 2007, 22: 288-289. |
[17]
|
García Castaño A, Pérez de Nanclares G, Madariaga L, et al. Poor phenotype-genotype association in a large series of patients with Type Ⅲ Bartter syndrome[J]. PloS One, 2017, 12: e0173581. doi: 10.1371/journal.pone.0173581 |
[18]
|
Palazzo V, Raglianti V, Landini S, et al. Clinical and genetic characterization of patients with Bartter and Gitelman syndrome[J]. Int J Mol Sci, 2022, 23: 5641. doi: 10.3390/ijms23105641 |
[19]
|
韩玥, 林毅, 孙清, 等. 中国16例巴特综合征基因变异分析和治疗随访研究[J]. 中华肾脏病杂志, 2017, 33: 573-581. doi: 10.3760/cma.j.issn.1001-7097.2017.08.003 |
[20]
|
Khandelwal P, Sabanadesan J, Sinha A, et al. Isolated nephrocalcinosis due to compound heterozygous mutations in renal outer medullary potassium channel[J]. CEN Case Rep, 2020, 9: 232-236. doi: 10.1007/s13730-020-00464-y |
[21]
|
王小娟, 陈琛, 杜婷婷, 等. 成年Ⅲ型Bartter综合征1例并文献复习[J]. 内科急危重症杂志, 2016, 22: 62-63. https://www.cnki.com.cn/Article/CJFDTOTAL-NKJW201601026.htm |
[22]
|
于迎, 潘晓霞, 任红, 等. 成人经典型Bartter综合征家系CLCNKB基因变异的研究[J]. 中华肾脏病杂志, 2010, 26: 598-602. doi: 10.3760/cma.j.issn.1001-7097.2010.08.007 |
[23]
|
韩玥, 王芳, 王彦刚, 等. 成年发病的2型巴特综合征1例[J]. 中华内科杂志, 2017, 56: 679-680. doi: 10.3760/cma.j.issn.0578-1426.2017.09.012 |
[24]
|
Huang L, Luiken GP, van Riemsdijk IC, et al. Nephrocalcinosis as adult presentation of Bartter syndrome type Ⅱ[J]. Neth J Med, 2014, 72: 91-93. |
[25]
|
Kleta R, Bockenhauer D. Salt-losing tubulopathies in children: what's new, what's controversial?[J]. J Am Soc Nephrol, 2018, 29: 727-739. doi: 10.1681/ASN.2017060600 |
[26]
|
Malafronte C, Borsa N, Tedeschi S, et al. Cardiac arrhythmias due to severe hypokalemia in a patient with classic Bartter disease[J]. Pediatr Nephrol, 2004, 19: 1413-1415. doi: 10.1007/s00467-004-1611-0 |
[27]
|
Cortesi C, Bettinelli A, Emma F, et al. Severe syncope and sudden death in children with inborn salt-losing hypokalaemic tubulopathies[J]. Nephrol Dial Transplant, 2005, 20: 1981-1983. doi: 10.1093/ndt/gfh893 |
[28]
|
Zanolari Calderari M, Vigier RO, Bettinelli A, et al. Electrocardiographic QT prolongation and sudden death in renal hypokalemic alkalosis[J]. Nephron, 2002, 91: 762-763. doi: 10.1159/000065045 |
[29]
|
Cortesi C, Lava SA, Bettinelli A, et al. Cardiac arrhythmias and rhabdomyolysis in Bartter-Gitelman patients[J]. Pediatr Nephrol, 2010, 25: 2005-2008. doi: 10.1007/s00467-010-1580-4 |
[30]
|
Blanchard A, Bockenhauer D, Bolignano D, et al. Gitelman syndrome: consensus and guidance from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference[J]. Kidney Int, 2017, 91: 24-33. doi: 10.1016/j.kint.2016.09.046 |
[31]
|
刘帆, 孙妍, 徐潮, 等. 低钾血症中遗传性肾小管疾病的临床特点分析[J]. 临床荟萃, 2021, 36: 436-441. doi: 10.3969/j.issn.1004-583X.2021.05.010 |
[32]
|
Walsh PR, Tse Y, Ashton E, et al. Clinical and diagnostic features of Bartter and Gitelman syndromes[J]. Clin Kidney J, 2018, 11: 302-309. doi: 10.1093/ckj/sfx118 |
[33]
|
韩玥, 郎艳华, 肖淑佼, 等. 中国5例2型巴特综合征KCNJ1基因变异分析和临床表型研究[J]. 中华肾脏病杂志, 2020, 36: 115-122. doi: 10.3760/cma.j.issn.1001-7097.2020.02.008 |
[34]
|
Bettinelli A, Borsa N, Bellantuono R, et al. Patients with biallelic mutations in the chloride channel gene CLCNKB: long-term management and outcome[J]. Am J Kidney Dis, 2007, 49: 91-98. doi: 10.1053/j.ajkd.2006.10.001 |
[35]
|
Scognamiglio R, Negut C, Calò LA. Aborted sudden cardiac death in two patients with Bartter's/Gitelman's syndromes[J]. Clin Nephrol, 2007, 67: 193-197. doi: 10.5414/CNP67193 |
[36]
|
Maruyama H, Shinno Y, Fujiwara K, et al. Nephrocal-cinosis and placental findings in neonatal bartter syndrome[J]. AJP Rep, 2013, 3: 21-24. |
[37]
|
Brochard K, Boyer O, Blanchard A, et al. Phenotype-genotype correlation in antenatal and neonatal variants of Bartter syndrome[J]. Nephrol Dial Transplant, 2009, 24: 1455-1464. doi: 10.1093/ndt/gfn689 |
[38]
|
李新岩, 姜艳, 许莉军, 等. KCNJ1新的复合杂合变异致Bartter综合征Ⅱ型临床和遗传分析[J]. 中华内科杂志, 2017, 56: 760-762. doi: 10.3760/cma.j.issn.0578-1426.2017.10.010 |
[39]
|
Yamazaki H, Nozu K, Narita I, et al. Atypical phenotype of type Ⅰ Bartter syndrome accompanied by focal segmental glomerulosclerosis[J]. Pediatr Nephrol, 2009, 24: 415-418. doi: 10.1007/s00467-008-0999-3 |
[40]
|
Adachi M, Tajima T, Muroya K, et al. Classic Bartter syndrome complicated with profound growth hormone deficiency: a case report[J]. J Med Case Rep, 2013, 7: 283. doi: 10.1186/1752-1947-7-283 |
[41]
|
Garnier ADS, Vargas-Poussou R, Oury JF, et al. Bartter syndrome prenatal diagnosis based on amniotic fluid biochemical analysis[J]. Pediatr Res, 2010, 67: 300-303. doi: 10.1203/PDR.0b013e3181ca038d |
[42]
|
Allaf B, Dreux S, Schmitz T, et al. Amniotic fluid biochemistry in isolated polyhydramnios: a series of 464 cases[J]. Prenat Diagn, 2015, 35: 1331-1335. doi: 10.1002/pd.4700 |
[43]
|
中国研究型医院学会罕见病分会, 中国罕见病联盟, 北京罕见病诊疗与保障学会, 等. Gitelman综合征诊疗中国专家共识(2021版)[J]. 协和医学杂志, 2021, 12: 902-912. doi: 10.12290/xhyxzz.2021-0555 |
[44]
|
Richards S, Aziz N, Bale S, et al. Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology[J]. Genet Med, 2015, 17: 405-424. doi: 10.1038/gim.2015.30 |
[45]
|
Marcoux AA, Slimani S, Tremblay LE, et al. Endocytic recycling of Na(+) -K(+) -Cl(-) cotransporter type 2: importance of exon 4[J]. J Physiol, 2019, 597: 4263-4276. doi: 10.1113/JP278024 |
[46]
|
Marcoux AA, Slimani S, Tremblay LE, et al. Regulation of Na(+)-K(+)-Cl(-) cotransporter type 2 by the with no lysine kinase-dependent signaling pathway[J]. Am J Physiol Cell Physiol, 2019, 317: 20-30. doi: 10.1152/ajpcell.00041.2019 |
[47]
|
彭晓艳, 蒋兰萍, 袁涛, 等. 氯离子清除试验在Gitelman综合征鉴别诊断中的应用[J]. 中国医学科学院学报, 2016, 38: 275-282. https://www.cnki.com.cn/Article/CJFDTOTAL-ZYKX201603006.htm |
[48]
|
Nozu K, Iijima K, Kanda K, et al. The pharmacological characteristics of molecular-based inherited salt-losing tubulopathies[J]. J Clin Endocrinol Metab, 2010, 95: 511-518. doi: 10.1210/jc.2010-0392 |
[49]
|
Colussi G, Bettinelli A, Tedeschi S, et al. A thiazide test for the diagnosis of renal tubular hypokalemic disorders[J]. Clin J Am Soc Nephrol, 2007, 2: 454-460. doi: 10.2215/CJN.02950906 |
[50]
|
Nam G, Cho A, Park MH. A rare cause of refractory severe polyhydramnios: antenatal Bartter syndrome[J]. Medicina, 2021, 57: 272. doi: 10.3390/medicina57030272 |
[51]
|
Dane B, Dane C, Aksoy F, et al. Antenatal Bartter syndrome: analysis of two cases with placental findings[J]. Fetal Pediatr Pathol, 2010, 29: 121-126. doi: 10.3109/15513811003777276 |
[52]
|
Bhat YR, Vinayaka G, Vani R, et al. Antenatal Bartter syndrome: a rare cause of unexplained severe polyhydra-mnios[J]. Ann Trop Paediatr, 2013, 31: 153-157. |
[53]
|
Mani S, Nair J, Handa D. Antenatal Bartter syndrome: a new compound heterozygous mutation in exon 2 of KCNJ1 gene[J]. BMJ Case Rep, 2021, 14: e244685. doi: 10.1136/bcr-2021-244685 |
[54]
|
Francini F, Gobbi L, Ravarotto V, et al. The dietary approach to the treatment of the rare genetic tubulopathies Gitelman's and Bartter's syndromes[J]. Nutrients, 2021, 13: 2960. doi: 10.3390/nu13092960 |
[55]
|
Han Y, Cheng H, Shao S, et al. Thirteen novel CLCNKB variants and genotype/phenotype association study in 42 Chinese patients with Bartter syndrome type 3[J]. Endocrine, 2020, 68: 192-202. doi: 10.1007/s12020-019-02156-9 |
[56]
|
Gasongo G, Greenbaum LA, Niel O, et al. Effect of nonsteroidal anti-inflammatory drugs in children with Bartter syndrome[J]. Pediatr Nephrol, 2019, 34: 679-684. doi: 10.1007/s00467-018-4135-8 |
[57]
|
Plumb LA, Van't Hoff W, Kleta R, et al. Renal apnoea: extreme disturbance of homoeostasis in a child with Bartter syndrome type Ⅳ[J]. Lancet, 2016, 388: 631-632. doi: 10.1016/S0140-6736(16)00087-8 |
[58]
|
Zaffanello M, Taranta A, Palma A, et al. Type Ⅳ Bartter syndrome: report of two new cases[J]. Pediatr Nephrol, 2006, 21: 766-770. doi: 10.1007/s00467-006-0090-x |
[59]
|
韩玥, 郎艳华, 林毅, 等. 中国4例4a型巴特综合征BSND基因变异和临床表型分析[J]. 中华肾脏病杂志, 2021, 37: 851-853. doi: 10.3760/cma.j.cn441217-20200915-00129 |
[60]
|
Adachi M, Asakura Y, Sato Y, et al. Novel SLC12A1 (NKCC2) mutations in two families with Bartter syndrome type 1[J]. Endocr J, 2007, 54: 1003-1007. doi: 10.1507/endocrj.K06-204 |
[61]
|
Nagao R, Suzuki S, Kawashima H, et al. Acute kidney injury in type 3 Bartter syndrome: angiotensin-converting enzyme inhibitors as a cause[J]. Pediatr Int, 2016, 58: 1373-1374. doi: 10.1111/ped.13100 |
[62]
|
Bell DS. Successful utilization of aliskiren, a direct renin inhibitor in Bartter syndrome[J]. South Med J, 2009, 102: 413-415. doi: 10.1097/SMJ.0b013e31819b8673 |
[63]
|
Seyberth HW, Schlingmann KP. Bartter- and Gitelman-like syndromes: salt-losing tubulopathies with loop or DCT defects[J]. Pediatr Nephrol, 2011, 26: 1789-1802. doi: 10.1007/s00467-011-1871-4 |
[64]
|
Kontorinis G, Giesemann AM, Iliodromiti Z, et al. Treating hearing loss in patients with infantile Bartter syndrome[J]. Laryngoscope, 2012, 122: 2524-2528. doi: 10.1002/lary.23532 |
[65]
|
Schurman SJ, Perlman SA, Sutphen R, et al. Genotype/phenotype observations in African Americans with Bartter syndrome[J]. J Pediatr, 2001, 139: 105-110. doi: 10.1067/mpd.2001.115020 |
[66]
|
Wu X, Yang G, Chen S, et al. Bartter syndrome with long-term follow-up: a case report[J]. J Int Med Res, 2020, 48: 300060520947876. |
[67]
|
Yang X, Zhang G, Wang M, et al. Bartter syndrome type 3: phenotype-genotype correlation and favorable response to ibuprofen[J]. Front Pediatr, 2018, 6: 153. doi: 10.3389/fped.2018.00153 |
[68]
|
Sardani Y, Qin K, Haas M, et al. Bartter syndrome complicated by immune complex nephropathy. Case report and literature review[J]. Pediatr Nephrol, 2003, 18: 913-918. doi: 10.1007/s00467-003-1194-1 |
[69]
|
Zhu B, Jiang H, Cao M, et al. A novel CLCNKB mutation in a Chinese girl with classic Bartter syndrome: a case report[J]. BMC Med Genet, 2019, 20: 137. doi: 10.1186/s12881-019-0869-9 |
[70]
|
Mrad FCC, Soares SBM, de Menezes Silva LAW, et al. Bartter's syndrome: clinical findings, genetic causes and therapeutic approach[J]. World J Pediatr, 2021, 17: 31-39. doi: 10.1007/s12519-020-00370-4 |
[71]
|
Landau D, Gurevich E, Sinai-Treiman L, et al. Accentua-ted hyperparathyroidism in type Ⅱ Bartter syndrome[J]. Pediatr Nephrol, 2016, 31: 1085-1090. doi: 10.1007/s00467-016-3337-1 |
[72]
|
Dickson FJ, Sayer JA. Nephrocalcinosis: a review of monogenic causes and insights they provide into this heterogeneous condition[J]. Int J Mol Sci, 2020, 21: 369. doi: 10.3390/ijms21010369 |
[73]
|
Devuyst O, Belge H, Konrad M, et al. Renal tubular disorders of electrolyte regulation in children[J]. Pediatr Nephrol, 2016, 38: 1246-1252. |
[74]
|
Landau D, Shalev L, Schneider E, et al. Bartter syndrome types 2 and 4: complications in currently treated young adults[J]. Pediatr Nephrol, 2016: 1743-1744. |
[75]
|
Saha A, Pande P, Vala K, et al. Clinical exome sequencing uncovers an unsuspected diagnosis of Bartter syndrome type 2 in a child with incidentally detected nephrocalcinosis[J]. CEN Case Rep, 2022, 11: 417-421. doi: 10.1007/s13730-022-00694-2 |
[76]
|
Tian M, Peng H, Bi X, et al. Late-onset Bartter syndrome type Ⅱ due to a novel compound heterozygous mutation in KCNJ1 gene: a case report and literature review[J]. Front Med, 2022, 9: 862514. doi: 10.3389/fmed.2022.862514 |
[77]
|
Sharma A, Linshaw MA. A novel compound heterozygous ROMK mutation presenting as late onset Bartter syndrome associated with nephrocalcinosis and elevated 1, 25(OH)(2) vitamin D levels[J]. Clin Exp Nephrol, 2011, 15: 572-576. doi: 10.1007/s10157-011-0431-3 |
[78]
|
Bettinelli A, Ciarmatori S, Cesareo L, et al. Phenotypic variability in Bartter syndrome type Ⅰ[J]. Pediatr Nephrol, 2000, 14: 940-945. doi: 10.1007/PL00013418 |
[79]
|
Hsu IR, Kamil ES, Lemley KV, et al. Syndrome of antenatal Bartter-like syndrome, hyperparathyroidism, hypercalcemia, bilateral nephrocalcinosis and nephrogenic DI in three patients treated with cinacalcet[J/OL ]. (2019-07-16)[2023-04-15]. https://doi.org/10.1093/edrv/35.supp.1. |
[80]
|
Novo R, Cartigny M, Lefevre C, et al. Bartter syndrome with bone-destroying hyperparathyroidism: about two cases, genetically proved, with long-lasting follow-up[J]. Horm Res Paediatr, 2016, 86: 173. |
[81]
|
Rodríguez-Soriano J, Vallo A, Aguirre M. Bone mineral density and bone turnover in patients with Bartter syndrome[J]. Pediatr Nephrol, 2005, 20: 1120-1125. doi: 10.1007/s00467-005-1901-1 |
[82]
|
Gross I, Siedner-Weintraub Y, Simckes A, et al. Antena-tal Bartter syndrome presenting as hyperparathyroidism with hypercalcemia and hypercalciuria: a case report and review[J]. J Pediatr Endocrinol Metab, 2015, 28: 943-946. |
[83]
|
He Y, Zhou Y, Wu W, et al. Bartter syndrome with multiple renal and liver cysts: a case report[J]. Int Urol Nephrol, 2022, 55: 225-228. doi: 10.1007/s11255-022-03274-6 |
[84]
|
Lee SE, Han KH, Jung YH, et al. Renal transplantation in a patient with Bartter syndrome and glomerulosclerosis[J]. Korean J Pediatr, 2011, 54: 36. doi: 10.3345/kjp.2011.54.1.36 |
[85]
|
Cha EJ, Hwang WM, Yun SR, et al. An adult case of Bartter syndrome type Ⅲ presenting with proteinuria[J]. J Pathol Transl Med, 2016, 50: 160-164. doi: 10.4132/jptm.2015.08.31 |
[86]
|
Carmody JB, Charlton JR. Short-term gestation, long-term risk: prematurity and chronic kidney disease[J]. Pediatrics, 2013, 131: 1168-1179. doi: 10.1542/peds.2013-0009 |
[87]
|
Chong L, Baikunje S, Poller DN, et al. An unusual cause of acute renal failure with volume depletion due to renal losses[J]. Am J Kidney Dis, 2008, 52: 366-369. doi: 10.1053/j.ajkd.2008.04.025 |
[88]
|
Khosravi M, Walsh SB. The long-term complications of the inherited tubulopathies: an adult perspective[J]. Pediatr Nephrol, 2014, 30: 385-395. |
[89]
|
Reinalter SC, Gröne HJ, Konrad M, et al. Evaluation of longterm treatment with indomethacin in hereditary hypokalemic salt-losing tubulopathies[J]. J Pediatr, 2001, 139: 398-406. doi: 10.1067/mpd.2001.117007 |
[90]
|
Altneida OD, Spinnato JA. Maternal Bartter's syndrome and pregnancy[J]. Am J Obstet Gynecol, 1989, 160: 1225-1226. doi: 10.1016/0002-9378(89)90198-1 |
[91]
|
Deruelle P, Dufour P, Magnenant E, et al. Maternal Bartter's syndrome in pregnancy treated by amiloride[J]. Eur J Obstet Gynecol Reprod Biol, 2004, 115: 106-107. doi: 10.1016/j.ejogrb.2004.01.030 |
[92]
|
O'Sullivan E, Monga M, Graves W. Bartter's syndrome in pregnancy: a case report and review[J]. Am J Perinatol, 1997, 14: 55-57. doi: 10.1055/s-2007-994097 |
[93]
|
Rigó J Jr, Gláz E, Papp Z. Low or high doses of spironolactone for treatment of maternal Bartter's syndrome[J]. Am J Obstet Gynecol, 1996, 174: 297. |
[94]
|
Nohira TNT, Akutagawa O, Fujito A, et al. Pregnancy complicated with Bartter's syndrome: a case report[J]. J Obstet Gynaecol Res, 2001, 27: 267-274. doi: 10.1111/j.1447-0756.2001.tb01268.x |
[95]
|
Luqman A, Kazmi A, Wall BM, et al. Bartter's syndrome in pregnancy: review of potassium homeostasis in gestation[J]. Am J Med Sci, 2009, 338: 500-504. doi: 10.1097/MAJ.0b013e31819f1ed8 |
[96]
|
Peregrin-Alvarez I, Rodriguez-Casares J, Lucena-Herrera C, et al. Bartter's syndrome and pregnancy[J]. Eur J Obstet Gynecol Reprod Biol, 2005, 121: 118-119. doi: 10.1016/j.ejogrb.2004.12.005 |
[97]
|
Zhang L, Peng X, Zhao B, et al. Clinical and laboratory features of female Gitelman syndrome and the pregnancy outcomes in a Chinese cohort[J]. Nephrology, 2020, 25: 749-757. doi: 10.1111/nep.13743 |
[98]
|
Kannan S, Delph Y, Moseley HS. Anaesthetic manage-ment of a child with Bartter's syndrome[J]. Can J Anaesth, 1995, 42: 808-812. doi: 10.1007/BF03011183 |
[99]
|
Raza D, Khan FA. Anaesthetic management for hiatal hernia repair in a child with Bartter's syndrome: A case report[J]. J Pak Med Assoc, 2020, 70: 737-739. |
[100]
|
Roelofse JA, van der Westhuijzen AJ. Anesthetic management of a patient with Bartter's syndrome undergoing orthognathic surgery[J]. Anesth Prog, 1997, 44: 71-75. |
[101]
|
Kim JY, Kim GA, Song JH, et al. A case of living-related kidney transplantation in Bartter's syndrome[J]. Yonsei Med J, 2000, 41: 662-665. doi: 10.3349/ymj.2000.41.5.662 |
[102]
|
Nooh N, Abdullah W, Sheta S. Anesthetic management of a patient with Bartter's syndrome undergoing bilateral sagittal split osteotomy[J]. Saudi J Anaesth, 2012, 6: 419-422. doi: 10.4103/1658-354X.105895 |
[103]
|
Fujino S, Miyoshi N, Ohue M, et al. Rectal cancer in a patient with Bartter syndrome: a case report[J]. Genes, 2017, 8: 139. doi: 10.3390/genes8050139 |
[104]
|
Gallagher H, Soar J, Tomson C. New guideline for perioperative management of people with inherited salt-wasting alkaloses[J]. Br J Anaesth, 2016, 116: 746-749. doi: 10.1093/bja/aew102 |