Клінічна характеристика та генетичний поліморфізм спадкової патології нирок. Повідомлення 1

Автор(и)

  • M. O. Ryznychuk
  • V. P. Pishak

DOI:

https://doi.org/10.24061/2413-0737.XVII.1.65.2013.40

Ключові слова:

спадкові нефропатії, нирки

Анотація

Наведено клінічні прояви найбільш поширених спадкових нефропатій з визначеннями типу успадкування.

Посилання

Bochkov NP. Klinicheskaya genetika [Clinical genetics]. Moscow: GEOTAR-MED; 2001. 448 р. (in Russian).

Baranov VS, Baranov EV, Ivashchenko TE, Aseev MV. Genom cheloveka i geny «predraspolozhennosti» [The human genome and the genes of "predisposition"]. St. Petersburg: Intermedika; 2000. 272 р.

Ozolinya LA, Efimov VS, Albulrab AS. Gipergomotsisteinemiya i akusherskaya patologiya [Hyperhomocysteinemia and obstetric pathology]. Rossiyskiy vestnik akusher-ginekologa. 2003;3(4):26-9. (in Russian).

Grechanina EYa, Grechanina YuB, Gol'dfarb IG. Khromosomnyy polimorfizm i metabolicheskie narusheniya – prichinno-sledstvennye svyazi [Chromosomal polymorphism and metabolic disorders - cause-effect relationships]. Ul'trazvukova perynatal'na diahnostyka. 2004;7:3-43. (in Russian).

Hrechanina OIa, Hrechanina YuB, Matalon RM. Porushennia obminu metioninu ta reproduktyvni vtraty (I chastyna) [Methionine metabolism disturbances and reproductive loss (Part I)]. Pediatriia, akusherstvo i hinekolohiia. 2009;71(4):69-74. (in Ukrainian).

Ignatova MS. Profilaktika nefropatiy i preduprezhdenie progressirovaniya bolezney pochek u detey [Prevention of nephropathy and prevention of kidney disease in children]. Rossiyskiy vestnik perinatologii i pediatrii. 2005;6:3-8. (in Russian).

Molchanova EA, Valov AL, Kabak MM. Pervye rezul'taty formirovaniya Rossiyskogo registra khronicheskoy pochechnoy nedostatochnosti u detey [The first results of the formation of the Russian registry of chronic renal failure in children]. Nefrologiya i dializ. 2004;5(1):64-8. (in Russian).

Novikov PV. Sostoyanie prenatal'noy diagnostiki vrozhdennykh i nasledstvennykh zabolevaniy v Rossiyskoy Federatsii [The state of prenatal diagnosis of congenital and hereditary diseases in the Russian Federation]. Akusherstvo i ginekologiya. 2006;2:3-7. (in Russian).

Ostrovskaya AV, Shefer K, Shtakkel'berg L. Evropeyskaya teratologicheskaya informatsionnaya sluzhba: opyt raboty, problemy, perspektivy [European Teratological Information Service: work experience, problems, prospects]. Pediatricheskaya farmakologiya. 2007;4(5):32-6. (in Russian).

Pishak VP, Myslyts'kyi VF, Tkachuk SS. Spadkovi syndromy z osnovamy fenotypovoi diahnostyky [Hereditary syndromes with the basics of phenotypic diagnosis]. Chernivtsi: Meduniversytet; 2010. 608 р. (in Ukrainian).

Fetisova IN, Dobrolyubov AS, Lipin MA, Polyakov AV. Polimorfizm genov folatnogo obmena i bolezni cheloveka [Polymorphism of folate metabolism genes and human diseases]. Vestnik novykh meditsinskikh tekhnologiy. 2007;10(1):47-54. (in Russian).

Pape L, Offner G, Ehrich J. A single center clinical experience in intensive care management of 104 pediatric renal transplantation between 1994 and 2002. Pediatric Transplantation. 2004;8:39-43.

Finishing the euchromatic segnence of the human genome. Nature. 2004;431:931-45.

Dolk H, Loane MA, Abramsky L. Response to Birth Prevalence of Congenital Heart Disease. Epidemiology. 2010;21(2):275-7.

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Опубліковано

2013-02-02

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