CERTAIN ASPECTS OF RESPIRATORY AND DIGESTIVE TRACT INVOLVEMENT IN CYSTIC FIBROSIS IN CHILDREN

Cystic fibrosis is one of the severe childhood disorders with early manifestation of multiple organ involvement. The respiratory and digestive tracts are suffered the most, the prognosis of disease course depends on the degree of the impairment of these systems.   The results of the analysis of cyst...

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Main Authors: T. G. Vasil’eva, S. N. Shishatskaya, A. N. Ni
Format: Article
Language:English
Published: "Paediatrician" Publishers LLC 2013-02-01
Series:Voprosy Sovremennoj Pediatrii
Subjects:
Online Access:https://vsp.spr-journal.ru/jour/article/view/385
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spelling doaj-ef39dd2e234e482ea16fd2729931b6e92021-07-28T21:15:31Zeng"Paediatrician" Publishers LLC Voprosy Sovremennoj Pediatrii1682-55271682-55352013-02-0112116216510.15690/vsp.v12i1.574385CERTAIN ASPECTS OF RESPIRATORY AND DIGESTIVE TRACT INVOLVEMENT IN CYSTIC FIBROSIS IN CHILDRENT. G. Vasil’eva0S. N. Shishatskaya1A. N. Ni2Territorial Centre of Specialized Medical Care, Vladivostok; Far Eastern Branch of the FSFI “Scientific Center of Family Health and Human Reproduction Problems” of the Siberian Department of RAMS, VladivostokVladivostok State Medical University, Russian FederationVladivostok State Medical UniversityCystic fibrosis is one of the severe childhood disorders with early manifestation of multiple organ involvement. The respiratory and digestive tracts are suffered the most, the prognosis of disease course depends on the degree of the impairment of these systems.   The results of the analysis of cystic fibrosis prevalence in Primorsky Krai according to the neonatal immunoreactive trypsin screening in 102 251 newborn are shown in the article. The age, sex, clinical and severity structure of cystic fibrosis was studied in 71 children. The prevalence of 13 mutations of transmembrane regulator conductance gene in 41 patients was determined. Correlations between time of pulmonary complications manifestation, P. Aeruginosa infection development, chronic hypoxemia degree, malnutrition, genetic status and severity of the disease were found.https://vsp.spr-journal.ru/jour/article/view/385cystic fibrosischildrenrespiratory tractdigestive tract
collection DOAJ
language English
format Article
sources DOAJ
author T. G. Vasil’eva
S. N. Shishatskaya
A. N. Ni
spellingShingle T. G. Vasil’eva
S. N. Shishatskaya
A. N. Ni
CERTAIN ASPECTS OF RESPIRATORY AND DIGESTIVE TRACT INVOLVEMENT IN CYSTIC FIBROSIS IN CHILDREN
Voprosy Sovremennoj Pediatrii
cystic fibrosis
children
respiratory tract
digestive tract
author_facet T. G. Vasil’eva
S. N. Shishatskaya
A. N. Ni
author_sort T. G. Vasil’eva
title CERTAIN ASPECTS OF RESPIRATORY AND DIGESTIVE TRACT INVOLVEMENT IN CYSTIC FIBROSIS IN CHILDREN
title_short CERTAIN ASPECTS OF RESPIRATORY AND DIGESTIVE TRACT INVOLVEMENT IN CYSTIC FIBROSIS IN CHILDREN
title_full CERTAIN ASPECTS OF RESPIRATORY AND DIGESTIVE TRACT INVOLVEMENT IN CYSTIC FIBROSIS IN CHILDREN
title_fullStr CERTAIN ASPECTS OF RESPIRATORY AND DIGESTIVE TRACT INVOLVEMENT IN CYSTIC FIBROSIS IN CHILDREN
title_full_unstemmed CERTAIN ASPECTS OF RESPIRATORY AND DIGESTIVE TRACT INVOLVEMENT IN CYSTIC FIBROSIS IN CHILDREN
title_sort certain aspects of respiratory and digestive tract involvement in cystic fibrosis in children
publisher "Paediatrician" Publishers LLC
series Voprosy Sovremennoj Pediatrii
issn 1682-5527
1682-5535
publishDate 2013-02-01
description Cystic fibrosis is one of the severe childhood disorders with early manifestation of multiple organ involvement. The respiratory and digestive tracts are suffered the most, the prognosis of disease course depends on the degree of the impairment of these systems.   The results of the analysis of cystic fibrosis prevalence in Primorsky Krai according to the neonatal immunoreactive trypsin screening in 102 251 newborn are shown in the article. The age, sex, clinical and severity structure of cystic fibrosis was studied in 71 children. The prevalence of 13 mutations of transmembrane regulator conductance gene in 41 patients was determined. Correlations between time of pulmonary complications manifestation, P. Aeruginosa infection development, chronic hypoxemia degree, malnutrition, genetic status and severity of the disease were found.
topic cystic fibrosis
children
respiratory tract
digestive tract
url https://vsp.spr-journal.ru/jour/article/view/385
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