Gender characteristics of the clinical manifestations of cardiovascular system involvement in X-linked Alport syndrome
https://doi.org/10.21508/1027-4065-2016-61-3-76-80
Abstract
About the Authors
O. S. GroznovaRussian Federation
Moscow
V. V. Dlin
Russian Federation
Moscow
L. I. Shagam
Russian Federation
Moscow
D. V. Shentseva
Russian Federation
Moscow
N. E. Konkova
Russian Federation
Moscow
References
1. Rana K., Tonna S., Wang Y.Y., et al. Nine novel COL4A3 and COL4A4 mutations and polymorphisms identified in inherited membrane diseases. Pediatr Nephrol 2007: 22; 652–657.
2. Hertz J.M., Thomassen M., Storey H., Flinter F. Clinical utility gene card for: Alport syndrome – update 2014. Eur J Hum Genet 2015; 23: 9: doi: 10.1038/ejhg.2014.254.
3. Savige J., Sheth S., Leys A. et al. Ocular features in Alport syndrome: pathogenesis and clinical significance. Clin J Am Soc Nephrol 2015; 10: 4: 703–709.
4. Miner J.H., Baigent C., Flinter F. et al. The 2014 International Workshop on Alport Syndrome. Kidney Int 2014; 86: 4: 679–684.
5. Kimberling W.J., Borsa N., Smith R.J. Hearing loss disorders associated with renal disease. Adv Otorhinolaryngol 2011; 70: 75–83.
6. Savige J., Ars E., Cotton R.G. et al. (The International Alport Mutation Consortium) DNA variant databases improve test accuracy and phenotype prediction in Alport syndrome. Pediatr Nephrol 2014; 29: 6: 971–977.
7. Lyons O.T.A., St. John E.R.C., Morales J.P. et al. Ruptured thoracoabdominal aortic aneurysm in a renal transplant patient with Alport’s syndrome. Ann Vasc Surg 2007; 21: 816–818.
8. Plaisier E., Gribouval O., Alamowitch S. et al. COL4A1 mutations and hereditary angiopathy, nephropathy, aneurysms, and muscle cramps. N Engl J Med 2007; 357: 2687–2695.
9. Шенцева Д.В., Грознова О.С., Длин В.В. и др. Поражение сердечно-сосудистой системы при синдроме Альпорта. Рос вестн перинатол и педиатр 2013; 3: 74–78. (Shentseva D.V., Groznova O.S., Dlin V.V. et al. Сardiovascular involvement in Alport syndrome. Ros vestn perinatol i pediatr 2013; 3: 74–78.)
10. Kashtan C.E., Segal Y., Flinter F. et al. Aortic abnormalities in males with Alport syndrome. Nephrol Dial Transplant 2010; 25: 11: 3554–3560.
11. Vogt B.A., Birk P.E., Panzarino V. et al. Aortic dissection in young patients with chronic hypertension. Am J Kidney Dis 1999; 33: 374–378.
12. Шенцева Д.В., Грознова О.С., Длин В.В. и др. Поражение сердечно-сосудистой системы у больных с синдромом Альпорта. Клин и экспер хир 2015; 2: 93–96. (Shentseva
13. D.V., Groznova O.S., Dlin V.V. et al. Сardiovascular involvement in patients with Alport syndrome. Klin ehksper hirur 2015; 2: 93–96.)
14. Kampmann C., Wiethoff C., Wenzel A. et al. Normal values of M mode echocardiographic measurements of more than 2000 healthy infants and children in central Europ Heart 2000; 83: 6: 667–672.
15. Warren A.E., Boyd M.L., O’Connell C., Dodds L. Dilatation of the ascending aorta in paediatric patients with bicuspid aortic valve: frequency, rate of progression and risk factors. Heart 2006; 92: 10: 1496–1500.
16. Gautier M., Detaint D., Fermanian C. et al. Nomograms for Aortic Root Diameters in Children Using Two-Dimensional Echocardiography. Am J Cardiol 2010; 105: 6: 888–894.
17. American Society of Echocardiography 2010 Guidelines http://aoroot.parameterz.com/.
18. Savige J., Gregory M., Gross O. et al. Expert guidelines for the management of Alport syndrome and thin basement membrane nephropathy. J Am Soc Nephrol 2013; 24: 3: 364–375.
19. Pierides A., Voskarides K., Kkolou M. et al. X-linked, COL4A5 hypomorphic Alport mutations such as G624D and P628L may only exhibit thin basement membrane nephropathy with microhematuria and late onset kidney failure. Hippokratia 2013; 17: 3: 207–213.
Review
For citations:
Groznova O.S., Dlin V.V., Shagam L.I., Shentseva D.V., Konkova N.E. Gender characteristics of the clinical manifestations of cardiovascular system involvement in X-linked Alport syndrome. Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics). 2016;61(3):76-80. (In Russ.) https://doi.org/10.21508/1027-4065-2016-61-3-76-80