Your browser does not allow JavaScript!
JavaScript is necessary for the proper functioning of this website. Please enable JavaScript or use a modern browser.
Open Science Slovenia
Open Science
DiKUL
slv
|
eng
Search
Browse
New in RUL
About RUL
In numbers
Help
Sign in
The genetic approach to stillbirth : a "systematic review"
ID
Dolanc Merc, Maja
(
Author
),
ID
Peterlin, Borut
(
Author
),
ID
Lovrečić, Luca
(
Author
)
PDF - Presentation file,
Download
(485,61 KB)
MD5: CC20DC0024FF73FE99AAD2C7162A8D4D
URL - Source URL, Visit
https://obgyn.onlinelibrary.wiley.com/doi/10.1002/pd.6354
Image galllery
Abstract
Unexplained stillbirth is defined as a stillbirth with no known cause after the exclusion of common causes, including obstetric complications, infections, placental insufficiency or abruption, umbilical cord complications, and congenital abnormalities with or without known genetic cause. More than 60% of stillbirth cases remain unexplained. The aim of this systematic review was to investigate the known genetic causes of unexplained stillbirth cases and to evaluate the current position and future directions for the use of genetic and genomic testing in expanding the knowledge in this field. A systematic search through several databases was performed using the keywords genetics and stillbirths in humans. Different methods to detect various types of causal genetic aberrations have been used in the past decades, from standard karyotyping to novel methods such as chromosomal microarray analysis and next generation sequencing technologies. Apart from common chromosomal aneuploidies, a promising hypothesis about genetic causes included genes related to cardiomyopathies and channelopathies. However, these were tested in the research settings, since molecular karyotyping is currently the standard approach in the routine evaluation of genetic causes of stillbirth. Hereby, we provide evidence that expanding knowledge using novel genetic and genomic testing might uncover new genetic causes of unexplained stillbirth.
Language:
English
Keywords:
stillbirth
,
genetic approach
,
genetics
,
human
Work type:
Article
Typology:
1.01 - Original Scientific Article
Organization:
MF - Faculty of Medicine
Publication status:
Published
Publication version:
Version of Record
Year:
2023
Number of pages:
Str. 1220-1228
Numbering:
Vol. 43, iss. 9
PID:
20.500.12556/RUL-155806
UDC:
575
ISSN on article:
0197-3851
DOI:
10.1002/pd.6354
COBISS.SI-ID:
192912643
Publication date in RUL:
19.04.2024
Views:
308
Downloads:
61
Metadata:
Cite this work
Plain text
BibTeX
EndNote XML
EndNote/Refer
RIS
ABNT
ACM Ref
AMA
APA
Chicago 17th Author-Date
Harvard
IEEE
ISO 690
MLA
Vancouver
:
Copy citation
Share:
Record is a part of a journal
Title:
Prenatal diagnosis
Shortened title:
Prenat. diagn.
Publisher:
Wiley
ISSN:
0197-3851
COBISS.SI-ID:
26168320
Licences
License:
CC BY-NC-ND 4.0, Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
Link:
http://creativecommons.org/licenses/by-nc-nd/4.0/
Description:
The most restrictive Creative Commons license. This only allows people to download and share the work for no commercial gain and for no other purposes.
Similar documents
Similar works from RUL:
Similar works from other Slovenian collections:
Back