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Naslov:Further exploration of cardiac channelopathy and cardiomyopathy genes in stillbirth
Avtorji:ID Dolanc Merc, Maja (Avtor)
ID Kotnik, Urška (Avtor)
ID Peterlin, Borut (Avtor)
ID Lovrečić, Luca (Avtor)
Datoteke:.pdf PDF - Predstavitvena datoteka, prenos (419,80 KB)
MD5: E410D4C29C90589773B2AA7708763014
 
URL URL - Izvorni URL, za dostop obiščite https://obgyn.onlinelibrary.wiley.com/doi/full/10.1002/pd.6616
 
Jezik:Angleški jezik
Tipologija:1.01 - Izvirni znanstveni članek
Organizacija:Logo UKC LJ - Univerzitetni klinični center Ljubljana
Povzetek:Objective: To explore genetic variation including whole genome copy numbervariation and sequence analysis of 98 genes associated with pediatric or adultcardiomyopathies, cardiac channelopathies, and sudden death in an unexplainedintrauterine fetal death cohort.Methods: The study population included 55 stillbirth cases that remained unex-plained after thorough postmortem examination, excluding maternal, fetal, andplacental causes of stillbirth. Molecular karyotyping was performed in 55 cases andthe trio exome sequencing approach was applied in 19 cases.Results: The analysis revealed six rare variants with predicted effects on proteinfunction in six genes (CASQ2, DSC2, KCNE1, LDB3, MYH6, and SCN5A) previouslyreported in cases of stillbirth or severe early onset pediatric cardiac related phe-notypes. When applying strict American College of Genetics and Genomics classi-fication guidelines, these are still variants of uncertain significance.Conclusions: Several potentially stillbirth-related genetic variants were detected inour cohort, adding to the growing literature on cardiac phenotype gene variation instillbirth. However, the mechanisms of action, gene-gene interaction, and contri-bution of the uterine environment are still to be deciphered. In order to advance ourknowledge of the genetics of unexplained fetal death, there is an evident need forinternational collaboration and field standardization
Ključne besede:stillbirth, genetic approach
Status publikacije:Objavljeno
Verzija publikacije:Objavljena publikacija
Leto izida:2024
Št. strani:str. 1062-1072
Številčenje:Letn. 44, št. 9
PID:20.500.12556/DiRROS-30315 Novo okno
UDK:575
ISSN pri članku:0197-3851
DOI:10.1002/pd.6616 Novo okno
COBISS.SI-ID:202250499 Novo okno
Datum objave v DiRROS:19.06.2026
Število ogledov:41
Število prenosov:28
Metapodatki:XML DC-XML DC-RDF
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Gradivo je del revije

Naslov:Prenatal diagnosis
Skrajšan naslov:Prenat Diagn
Založnik:Wiley
ISSN:0197-3851
COBISS.SI-ID:26168320 Novo okno

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Licenca:CC BY-NC-ND 4.0, Creative Commons Priznanje avtorstva-Nekomercialno-Brez predelav 4.0 Mednarodna
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