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Ugotavljanje genetskega ozadja hipoholesterolemije in povezav s kliničnimi značilnostmi pri otrocih in mladostnikih
ID Molk, Neža (Author), ID DEBELJAK, MARUŠA (Mentor) More about this mentor... This link opens in a new window, ID Grošelj, Urh (Co-mentor)

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Abstract
Dislipidemije povzročajo neravnovesje lipoproteinov v krvi. Njihova zgodnja diagnoza in zdravljenje sta ključnega pomena, saj sta pomemben dejavnik tveganja za razvoj srčno-žilnih bolezni. Primarne hipoholesterolemije so manj raziskana skupina dislipidemij. Zanje so značilne vrednosti celokupnega holesterola in LDL holesterola (LDL) pod 5. percentilom splošne populacije. Zgodnja diagnoza primarnih hipoholesterolemij je pomembna predvsem pri pacientih, ki imajo zaradi hipoholesterolemije nižje vrednosti lipidotopnih vitaminov. V magistrski nalogi smo raziskali genetsko ozadje hipoholesterolemij v skupini 46 otrok in mladostnikov z izmerjenimi nižjimi vrednostmi holesterola. S sekvenciranjem naslednje generacije smo določili zaporedja vseh kodirajočih elementov človeškega genoma. Analizirali smo spremembe v panelu 28 genov povezanih z nižjimi vrednostmi holesterola. Slabše pokrite spremembe smo dodatno potrjevali s sekvenciranjem po Sangerju. Pri 13 preiskovancih smo potrdili prisotnost vzročne patološke spremembe. V primerih, kjer genetskega vzroka hipoholesterolemije nismo našli, ne izključujemo možnosti obstoja sekundarnega vzroka hipoholesterolemije ali prisotnosti sprememb v drugih genih ali regijah, ki niso bili vključeni v raziskavo.

Language:Slovenian
Keywords:hipoholesterolemija, holesterol, dislipidemija, genetski vzroki hipoholesterolemije, sekvenciranje naslednje generacije
Work type:Master's thesis/paper
Typology:2.09 - Master's Thesis
Organization:BF - Biotechnical Faculty
Year:2023
PID:20.500.12556/RUL-152564 This link opens in a new window
COBISS.SI-ID:174343939 This link opens in a new window
Publication date in RUL:29.11.2023
Views:404
Downloads:30
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Secondary language

Language:English
Title:Assessment of genetic background of hypocholesterolemia and correlations with clinical characteristics in children and adolescents
Abstract:
Early diagnosis and treatment of dyslipidemias are crucial as they disrupt the balance of lipoproteins in the blood and pose a significant risk for cardiovascular diseases. Primary hypocholesterolemias are a less known group of dyslipidemias, where total cholesterol and LDL cholesterol (LDL) values fall below the 5th percentile of the general population. Early diagnosis of primary hypocholesterolemia is especially vital for individuals with concentrations of lipid-soluble vitamins. In our study, we researched the genetic background of 46 children and adolescents with lower cholesterol levels. We performed whole exome sequencing and examined 28 genes linked to reduced cholesterol levels. We found pathogenic variants in 13 probands, some of which have not been described in the literature yet. For cases without an identified genetic cause, there might be secondary factors or changes in other genes or regions beyond our study's scope.

Keywords:hypocholesterolemia, cholesterol, dyslipidemia, genetic causes of hypocholesterolemia, next generation sequencing

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