参考文献

［1］梅长林，余学清.国家卫生和计划生育委员会住院医师规范化培训教材：内科学·肾脏内科分册［M］.北京：人民卫生出版社，2015.

［2］林果为，王吉耀，葛均波.实用内科学［M］.15版.北京：人民卫生出版社，2017.

［3］FEEHALLY F, FLOEGE J, TONELLI M, et al.Comprehensive clinical nephrology[M].6th ed.United States of America: Elsevier, 2019.

［4］TAAL M W, TAAL M W, TAAL M W, et al.Brenner and Rector’s The Kidney[M].11th ed.United States of America: Elsevier, 2020.

［5］TRYGGVASON K, PATRAKKA J.Thin basement membrane nephropathy[J].J Am Soc Nephrol,2006, 17(3): 813—822.

［6］SAVIGE J, RANA K, TONNA S, et al.Thin basement membrane nephropathy[J].Kidney Int,2003, 64(4): 1169—1178.

［7］BUZZA M, WILSON D, SAVIGE J.Segregation of hematuria in thin basement membrane disease with haplotypes at the loci for Alport syndrome[J].Kidney Int, 2001, 59(5): 1670—1676.

［8］VOSKARIDES K, DAMIANOU L, NEOCLEOUS V, et al.COL4A3/COL4A4 mutations producing focal segmental glomerulosclerosis and renal failure in thin basement membrane nephropathy[J].J Am Soc Nephrol, 2007, 18(11): 3004—3016.(https://www.daowen.com)

［9］ANDREAS M, TSIELESTINA P, JOURNAL D C J C K.Prevalence of clinical, pathological and molecular features of glomerular basement membrane nephropathy caused by COL4A3 or COL4A4 mutations: a systematic review[J].2020, 13(6): 1025—1036.

［10］章友康，周蓉，王素霞.薄基底膜肾病27例研究［J］.中华内科杂志，1997，11：736—739.

［11］QAZI R A, BASTANI B.Co-existence of thin basement membrane nephropathy with other glomerular pathologies；a single center experience[J].Journal of nephropathology, 2015, 4(2):43—47.

［12］SAVIGE J, GREGORY M, GROSS O, et al.Expert guidelines for the management of Alport syndrome and thin basement membrane nephropathy[J].J Am Soc Nephrol, 2013, 24(3):364—375.

［13］CHURG J B J, GLASSOCK R J.Renal disease: classification and atlas of glomerular diseases[M].2nd ed.New York: Igaku—Shoin Medical Publishers, 1995.

［14］LI Y, GROOPMAN E E, D’AGATI V, et al.Type Ⅳ collagen mutations in familial IgA nephropathy[J].Kidney Int Rep, 2020, 5(7): 1075—1078.

［15］SAVIGE J, STOREY H, WATSON E, et al.Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria[J].Eur J Hum Genet,2021.