The Genetics of Non-Syndromic Primary Ovarian Insufficiency: A Systematic Review.
Genetic
Gynecology
Molecular
Precision Medicine
Journal
International journal of fertility & sterility
ISSN: 2008-076X
Titre abrégé: Int J Fertil Steril
Pays: Iran
ID NLM: 101487941
Informations de publication
Date de publication:
Oct 2019
Oct 2019
Historique:
received:
29
06
2018
accepted:
15
01
2019
entrez:
17
7
2019
pubmed:
17
7
2019
medline:
17
7
2019
Statut:
ppublish
Résumé
Several causes for primary ovarian insufficiency (POI) have been described, including iatrogenic and environmental factor, viral infections, chronic disease as well as genetic alterations. The aim of this review was to collect all the genetic mutations associated with non-syndromic POI. All studies, including gene screening, genome-wide study and assessing genetic mutations associated with POI, were included and analyzed in this systematic review. Syndromic POI and chromosomal abnormalities were not evaluated. Single gene perturbations, including genes on the X chromosome (such as
Identifiants
pubmed: 31310068
doi: 10.22074/ijfs.2019.5599
pmc: PMC6642427
doi:
Types de publication
Systematic Review
Langues
eng
Pagination
161-168Informations de copyright
Copyright© by Royan Institute. All rights reserved.
Déclaration de conflit d'intérêts
The authors declare no conflicts of interest.
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