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The clinical case of the child with cystic fibrosis and multiple organ failure syndrome development

Клінічний випадок муковісцидозу із розвитком синдрому поліорганної недостатності у дитини
Authors: Drobova, N.M.; Yanovska, K.O.; Pasichnyk, O.V.; Klymenko, V.A.; Piontkovska, O.V.; Bevz, S.I.; Sindeeva, N.T.;

The clinical case of the child with cystic fibrosis and multiple organ failure syndrome development

Abstract

Представлен клинический случай муковисцидоза у ребенка, который был носителем тяжелой мутации гена муковисцидоза delF508 и умер от развития синдрома полиорганной недостаточности в возрасте 17 лет.

Наведений клінічний випадок муковісцидозу у дитини, яка була носієм важкої мутації гена муковісцидозу delF508 та померла від розвитку синдрому поліорганної недостатності у віці 17 років.

The clinical case of the child with cystic fibrosis and severe delF508 CFTR mutation is described in the article. This patient died from multiorgan failure syndrome at 17 years old.

Keywords

муковисцидоз; дети; цирроз печени; синдром полиорганной недостаточности, муковісцидоз; діти; цироз печінки; синдром поліорганної недостатності, children; cystic fibrosis; liver cirrhosis; multiorgan failure syndrome

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
0
Average
Average
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