Genetic factors of hereditary phenotypes of vesicoureteral reflux and reflux nephropathy
The article reviews publications on genetically determined vesicoureteral reflux and reflux nephropathy, accompanying certain phenotypes of systemic or local forms of hereditary connective tissue dysplasia (Ehlers–Danlo, Marfan, Williams syndromes, sluggish skin). The authors determined the role of...
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Ltd. “The National Academy of Pediatric Science and Innovation”
2020-07-01
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| Series: | Rossijskij Vestnik Perinatologii i Pediatrii |
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| Online Access: | https://www.ped-perinatology.ru/jour/article/view/1147 |
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doaj-06655fee88394a6dbbdd3d54f8bd0de82021-07-28T16:27:53ZrusLtd. “The National Academy of Pediatric Science and Innovation”Rossijskij Vestnik Perinatologii i Pediatrii1027-40652500-22282020-07-01653323810.21508/1027-4065-2020-65-3-32-38885Genetic factors of hereditary phenotypes of vesicoureteral reflux and reflux nephropathyE. A. Yuryeva0V. V. Dlin1E. S. Vozdvizhenskaya2Veltischev Research and Clinical Institute for Pediatrics of the Pirogov Russian National Research Medical UniversityVeltischev Research and Clinical Institute for Pediatrics of the Pirogov Russian National Research Medical UniversityVeltischev Research and Clinical Institute for Pediatrics of the Pirogov Russian National Research Medical UniversityThe article reviews publications on genetically determined vesicoureteral reflux and reflux nephropathy, accompanying certain phenotypes of systemic or local forms of hereditary connective tissue dysplasia (Ehlers–Danlo, Marfan, Williams syndromes, sluggish skin). The authors determined the role of mutations of the genes of fibrillar collagen, elastin, transforming growth factor β1, tenascin, lysyl peroxidase, metalloproteinases and other components of connective tissue, as well as their possible combination in the development of pathology. The authors call the specialists to continue research on genetic mutations in vesicoureteral reflux and reflux nephropathy.https://www.ped-perinatology.ru/jour/article/view/1147childrenvesicoureteral refluxreflux nephropathygenetic factorsehlers–danlomarfanwilliams syndromessluggish skin (cutis laxa) |
| collection |
DOAJ |
| language |
Russian |
| format |
Article |
| sources |
DOAJ |
| author |
E. A. Yuryeva V. V. Dlin E. S. Vozdvizhenskaya |
| spellingShingle |
E. A. Yuryeva V. V. Dlin E. S. Vozdvizhenskaya Genetic factors of hereditary phenotypes of vesicoureteral reflux and reflux nephropathy Rossijskij Vestnik Perinatologii i Pediatrii children vesicoureteral reflux reflux nephropathy genetic factors ehlers–danlo marfan williams syndromes sluggish skin (cutis laxa) |
| author_facet |
E. A. Yuryeva V. V. Dlin E. S. Vozdvizhenskaya |
| author_sort |
E. A. Yuryeva |
| title |
Genetic factors of hereditary phenotypes of vesicoureteral reflux and reflux nephropathy |
| title_short |
Genetic factors of hereditary phenotypes of vesicoureteral reflux and reflux nephropathy |
| title_full |
Genetic factors of hereditary phenotypes of vesicoureteral reflux and reflux nephropathy |
| title_fullStr |
Genetic factors of hereditary phenotypes of vesicoureteral reflux and reflux nephropathy |
| title_full_unstemmed |
Genetic factors of hereditary phenotypes of vesicoureteral reflux and reflux nephropathy |
| title_sort |
genetic factors of hereditary phenotypes of vesicoureteral reflux and reflux nephropathy |
| publisher |
Ltd. “The National Academy of Pediatric Science and Innovation” |
| series |
Rossijskij Vestnik Perinatologii i Pediatrii |
| issn |
1027-4065 2500-2228 |
| publishDate |
2020-07-01 |
| description |
The article reviews publications on genetically determined vesicoureteral reflux and reflux nephropathy, accompanying certain phenotypes of systemic or local forms of hereditary connective tissue dysplasia (Ehlers–Danlo, Marfan, Williams syndromes, sluggish skin). The authors determined the role of mutations of the genes of fibrillar collagen, elastin, transforming growth factor β1, tenascin, lysyl peroxidase, metalloproteinases and other components of connective tissue, as well as their possible combination in the development of pathology. The authors call the specialists to continue research on genetic mutations in vesicoureteral reflux and reflux nephropathy. |
| topic |
children vesicoureteral reflux reflux nephropathy genetic factors ehlers–danlo marfan williams syndromes sluggish skin (cutis laxa) |
| url |
https://www.ped-perinatology.ru/jour/article/view/1147 |
| work_keys_str_mv |
AT eayuryeva geneticfactorsofhereditaryphenotypesofvesicoureteralrefluxandrefluxnephropathy AT vvdlin geneticfactorsofhereditaryphenotypesofvesicoureteralrefluxandrefluxnephropathy AT esvozdvizhenskaya geneticfactorsofhereditaryphenotypesofvesicoureteralrefluxandrefluxnephropathy |
| _version_ |
1721266153346564096 |