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Kurzyńska, Anna
2023
Praca doktorska
Molecular testing is one of the key and rapidly developing diagnostic methods in modern endocrinology. Searching for genetic alterations not only makes it possible to establish the proper diagnosis or predict the clinical course of a given disease entity, but can also provide opportunities for therapy, especially in the era of personalized medicine. The purpose of this dissertation was to address issues related to genetic testing in selected rare endocrine disorders. Objects of the study: 1. A high correlation between genotype and phenotype in patients with the classical form of congenital adrenal hyperplasia caused by 21-hydroxylase deficiency. A novel pathogenic variant of CYP21A2 previously not reported in the literature, was identified and characterized. 2. Assess the significance of selected single nucleotide genetic variants in the susceptibility and clinical course of neuroendocrine tumors. 3. Linking the atypical clinical course of aggressive hereditary paraganglioma to a pathogenic variant in the SDHD gene, previously described as of "uncertain clinical significance".
Kraków
2 - studia doktoranckie
endokrynologia
Rada Dyscypliny Nauki medyczne
Przybylik-Mazurek, Elwira
2022
oai:dl.cm-uj.krakow.pl:4987
ZB-137598
pol; eng
nieograniczony
9 lis 2023
26 paź 2023
51
46
http://dl.cm-uj.krakow.pl:8080/publication/4988
RDF
OAI-PMH
Lenda-Tracz, Wioletta
Gryzło, Beata
Zaręba, Paula
Styl cytowania: chicago-author-date iso690-author-date
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