nefrНефрологияNephrology (Saint-Petersburg)1561-62742541-9439Pavlov First Saint-Petersburg State Medical University10.24884/1561-6274-2008-12-3-99-109nefr-1125Research ArticleПРОГРАММА НЕПРЕРЫВНОГО ПОСЛЕДИПЛОМНОГО ОБРАЗОВАНИЯ ПО НЕФРОЛОГИИPROGRAM ON CONTINUOUS POSTGRADUATE EDUCATION ON NEPHROLOGYРЕДКИЕ ЗАБОЛЕВАНИЯ В ПРАКТИКЕ «ВЗРОСЛОГО» НЕФРОЛОГА: НАСЛЕДСТВЕННЫЙ НЕФРИТ (СИНДРОМ АЛЬПОРТА), БОЛЕЗНЬ ТОНКОЙ БАЗАЛЬНОЙ МЕМБРАНЫ, ОЛИГОМЕГАНЕФРОНИЯRARE DISEASES IN THE PRACTICE OF «ADULT» NEPHROLOGISTS: INHERITED NEPHRITIS (ALPORT SYNDROME), THE THIN BASEMENT MEMBRANE DISEASE, OLIGOMEGANEPHRONIAКаюковИ. Г.KayukovI. G.

кафедра нефрологии и диализа

197022 Санкт-Петербург, ул. Л.Толстого 17, СПбГМУ им. акад. И.П. Павлова, Нефрокорпус, тел.: 812-3463926; факс: 812-2349191

kaukov@nephrolog.ruЕсаянА. М.EssaianA. M.

кафедра нефрологии и диализа

СмирновА. В.SmirnovA. V.

кафедра пропедевтики  внутренних болезней

СиповскийВ. Г.SipovskyV. G.

Научно-исследовательский институт нефрологии

КучерА. Г.KucherA. G.

кафедра пропедевтики внутренних болезней

Санкт-Петербургский государственный медицинский университет им. акад. И.П. ПавловаRussian Federation20081003200812399109Copyright © Каюков И.Г., Есаян А.М., Смирнов А.В., Сиповский В.Г., Кучер А.Г., 20082008Каюков И.Г., Есаян А.М., Смирнов А.В., Сиповский В.Г., Кучер А.Г.Kayukov I.G., Essaian A.M., Smirnov A.V., Sipovsky V.G., Kucher A.G.Данная работа распространяется под лицензией Creative Commons Attribution 4.0.This work is licensed under a Creative Commons Attribution 4.0 License.https://journal.nephrolog.ru/jour/article/view/1125

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наследственный нефритсиндром Альпортаболезнь тонкой базальной мембраныолигомеганефрониядиагностикалечениеinherited nephritisAlport syndromethe thin basement membrane diseaseoligomeganephroniadiagnosticstreatmentReferencesOMIM. Online Mendelian Inheretence in Man. http://www.ncbi.nlm.nih.gov/sites/entrezOMIM. Online Mendelian Inheretence in Man. http://www.ncbi.nlm.nih.gov/sites/entrezИгнатова МС, Вельтищев ЮЕ. Детская нефрология. Л., Медицина, 1989; 445Игнатова МС, Вельтищев ЮЕ. Детская нефрология. Л., Медицина, 1989; 445Appel GB, Radhakrishnan J, D’Agati V. Secondary glomerular disease. In: Brenner BM, ed. The Kidney, sixth edition, 2000, W. B. Saunders, Philadelphia et al.; 1350-1448Appel GB, Radhakrishnan J, D’Agati V. Secondary glomerular disease. In: Brenner BM, ed. The Kidney, sixth edition, 2000, W. B. Saunders, Philadelphia et al.; 1350-1448Gubler MC. Inherited diseases of the glomerular basement membrane. Nat Clin Pract Nephrol 2008;4(1): 24-37Gubler MC. Inherited diseases of the glomerular basement membrane. Nat Clin Pract Nephrol 2008;4(1): 24-37Clifford E, Kashtan MD, Alfred F, Michael MD. Alport syndrome: From bedside to genome to bedside. Am J Kidney Dis 1993; 5: 627-640Clifford E, Kashtan MD, Alfred F, Michael MD. Alport syndrome: From bedside to genome to bedside. Am J Kidney Dis 1993; 5: 627-640Heath KE, Campos-Barros A, Toren A et al. Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromes. Am J Hum Genet 2001; 69: 1033-1045Heath KE, Campos-Barros A, Toren A et al. Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromes. Am J Hum Genet 2001; 69: 1033-1045Kashtan CE. Alport syndrome and the X-chromosome: implications of a diagnosis of Alport syndrome in females. Nephrol Dial Transplant 2007; 22: 1499-1505Kashtan CE. Alport syndrome and the X-chromosome: implications of a diagnosis of Alport syndrome in females. Nephrol Dial Transplant 2007; 22: 1499-1505Kashtan CE. Renal transplantation in patients with Alport syndrome. Pediatr Transplantation 2006; 10: 651-657Kashtan CE. Renal transplantation in patients with Alport syndrome. Pediatr Transplantation 2006; 10: 651-657Tryggvason K, Patrakka J. Thin basement membrane nephropathy. J Am Soc Nephrol 2006; 17: 813-822Tryggvason K, Patrakka J. Thin basement membrane nephropathy. J Am Soc Nephrol 2006; 17: 813-822Welling LW, Granthem JJ. Cystic and developmental diseases of kidney. In; Brenner BM, ed. Вrenner & Rector. The Kydney 4 th ed. Saunderas, Philadelphia et al, 1998: Vol. 2, Chap. 38Welling LW, Granthem JJ. Cystic and developmental diseases of kidney. In; Brenner BM, ed. Вrenner & Rector. The Kydney 4 th ed. Saunderas, Philadelphia et al, 1998: Vol. 2, Chap. 38Potter EL. Normal and abnormal development of the kidney. Medical Publishers, Chicago, 1972Potter EL. Normal and abnormal development of the kidney. Medical Publishers, Chicago, 1972Schwarz RD, Stephens FD, Cussen LJ. The pathogenesis of renal dysplasia. III. Complete and incomplete urinary obstruction. Invest Urol 1981; 19: 101-105Schwarz RD, Stephens FD, Cussen LJ. The pathogenesis of renal dysplasia. III. Complete and incomplete urinary obstruction. Invest Urol 1981; 19: 101-105Salomon R, Tellier AL, Bitach TA. PAX2 mutations in oligomeganephronia. Kidney Int 2001; 59: 457-461Salomon R, Tellier AL, Bitach TA. PAX2 mutations in oligomeganephronia. Kidney Int 2001; 59: 457-461Drukker A. Oligonephropathy: from a rare childhood disorder to a possible health problem in the adult. Isr Med Assoc J 2002; 4 (3): 191-195Drukker A. Oligonephropathy: from a rare childhood disorder to a possible health problem in the adult. Isr Med Assoc J 2002; 4 (3): 191-195

The authors declare that there are no conflicts of interest present.