Staphylococcal scalded skin syndrome in the Czech Republic: an epidemiological study

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14110%2F12%3A00059356" target="_blank" >RIV/00216224:14110/12:00059356 - isvavai.cz</a>

Nalezeny alternativní kódy

RIV/65269705:_____/12:#0002021

Výsledek na webu

<a href="http://dx.doi.org/10.1016/j.burns.2011.08.005" target="_blank" >http://dx.doi.org/10.1016/j.burns.2011.08.005</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1016/j.burns.2011.08.005" target="_blank" >10.1016/j.burns.2011.08.005</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Staphylococcal scalded skin syndrome in the Czech Republic: an epidemiological study

Popis výsledku v původním jazyce

Objective To identify the basic epidemiological characteristics of children hospitalized with diagnosis of Staphylococcal scalded skin syndrome in the Czech Republic in the years 1994?2009. Introduction Staphylococcal scalded skin syndrome (SSSS) is a relatively rare disease in childhood. This syndrome was first defined in 1878 by Baron Gottfried Ritter von Rittershainem and belongs to the group of diseases called Burn-like syndromes. It is a bullous skin disease caused by exfoliative toxins which are produced by certain types of Staphyloccocus aureus. Typical structures affected by these toxins are desmosome proteins called Desmoglein-1 located in the stratum granulosum of epidermis. Unlike in Lyell's syndrome or Stevens-Johnson's syndrome, the exfoliation is caused by loss of adhesivity particularly in the stratum granulosum and not by induction of apoptosis in the dermo-epidermal junction.

Název v anglickém jazyce

Staphylococcal scalded skin syndrome in the Czech Republic: an epidemiological study

Popis výsledku anglicky

Objective To identify the basic epidemiological characteristics of children hospitalized with diagnosis of Staphylococcal scalded skin syndrome in the Czech Republic in the years 1994?2009. Introduction Staphylococcal scalded skin syndrome (SSSS) is a relatively rare disease in childhood. This syndrome was first defined in 1878 by Baron Gottfried Ritter von Rittershainem and belongs to the group of diseases called Burn-like syndromes. It is a bullous skin disease caused by exfoliative toxins which are produced by certain types of Staphyloccocus aureus. Typical structures affected by these toxins are desmosome proteins called Desmoglein-1 located in the stratum granulosum of epidermis. Unlike in Lyell's syndrome or Stevens-Johnson's syndrome, the exfoliation is caused by loss of adhesivity particularly in the stratum granulosum and not by induction of apoptosis in the dermo-epidermal junction.

Druh

J_x - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)

CEP obor

FE - Ostatní obory vnitřního lékařství

OECD FORD obor

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Projekt

—

Návaznosti

I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Rok uplatnění

2012

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Burns

ISSN

0305-4179

e-ISSN

—

Svazek periodika

38

Číslo periodika v rámci svazku

2

Stát vydavatele periodika

GB - Spojené království Velké Británie a Severního Irska

Počet stran výsledku

5

Strana od-do

296-300

Kód UT WoS článku

000301621500021

EID výsledku v databázi Scopus

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