[1] Haque SK1, Ariceta G, Batlle D,et al.Proximal renal tubular acidosis: a not so rare disorder of multiple etiologies[J].Nephrol Dial Transplant,2012,27(12): 4273-4287. [2] 邵怡,王安平,王先令,等.肾小管酸中毒的诊疗进展[J].国际内分泌代谢杂志,2017,37(1):56- 58. [3] 江载芳,申昆玲,沈颖.诸福棠实用儿科学[M].第8版.北京:人民卫生出版社, 2014. [4] 黄文彦,孙蕾.儿童先天/遗传性肾小管疾病诊断与治疗现状[J].中华实用儿科临床杂志,2015,30(17):1285-1288. [5] Zhang J.Incomplete distalrenal tubular acidosis from a heterozygou B1 subunit s mutation of the V-ATPase[J].Am J Physiol Renal Physiol,2014,307(9): 1063-1071. [6] Karunarathne S, Udayakumara Y, Govindapala D,et al. Medullary nephrocalcinosis, distal renal tubular acidosis and polycythaemia in a patient with nephrotic syndrome[J].BMC Nephrol,2012, 13(7):66-70. [7] Sharma S, Gupta A, Saxena S. Comprehensive clinical approach to renal tubular acidosis[J].Clin Exp Nephrol,2015, 19(4):556-561. [8] 涂娟,陈朝英.41 例儿童肾小管酸中毒的临床分析[J].中国医刊,2016,51(6)67-70. [9] Sharma S, Gupta A, Saxena S. Comprehensive clinical approach to renal tubular acidosis[J].Clin Exp Nephrol,2015, 19(4):556-561. [10] Hamnvik OP,Vaidya A,Becker C.Interactive medical case:wasting away[J].N Engl J Med,2014,370(7):e12. [11] Santos F,Ordonez FA,Claramunt-Taberner D,et al.Clinical and laboratory approaches in the diagnosis of renal tubular acidosis[J].Pediatr Nephrol,2015,30(12):2099-2107. [12] An den Wildenberg MJ,Hoorn EJ,Mohebbi N,et al.Distal renal tubular acidosis with multiorgan autoimmunity: a case report [J].Am J Kidney Dis,2015,65(4):607-610. [13] Zhang C,Ren H,Shen P,et al.Clinical evaluation of Chinese patients with primary distal renal tubular acidosis[J].Intern Med,2015,54(7):725-730. (本文编辑:邓丽萍) [收稿日期] 2017-09-18
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