Results 11 to 20 of about 4,572,851 (176)

Preimplantation Genetic Testing for Monogenic Kidney Disease [PDF]

open access: yesClinical Journal of the American Society of Nephrology, 2020
Background and objectives A genetic cause can be identified for an increasing number of pediatric and adult-onset kidney diseases. Preimplantation genetic testing (formerly known as preimplantation genetic diagnostics) is a reproductive technology that helps prospective parents to prevent passing on (a) disease ...
Rozemarijn Snoek   +11 more
openaire   +7 more sources

Targeting myotonic dystrophy by preimplantation genetic diagnosis-karyomapping

open access: yesTaiwanese Journal of Obstetrics & Gynecology, 2019
Objective: To report a case with Myotonic dystrophy type I with successful preimplantation genetic diagnosis-karyomapping. Case report: A 34-year-old female carrier of myotonic dystrophy type I was treated at our clinic with a successful pregnancy after ...
Cheng-Wei Wang   +2 more
doaj   +2 more sources

Non-Invasive Preimplantation Genetic Testing

open access: yesGenes
To minimise the influence of chromosomal abnormalities during IVF treatment, embryos can be screened before transfer using preimplantation genetic testing. This typically involves an invasive trophectoderm biopsy at the blastocyst stage, where 4-8 cells are collected and analysed.
Daniela N. Bakalova   +2 more
openaire   +3 more sources

Preimplantation genetic testing: Its evolution, where are we today?

open access: yesJournal of Human Reproductive Sciences, 2018
Preimplantation genetic testing (PGT) is an early form of prenatal genetic diagnosis where abnormal embryos are identified, thereby allowing transfer of genetically normal embryos.
Firuza Rajesh Parikh   +5 more
doaj   +2 more sources

Clinical Applications of Preimplantation Genetic Testing in Equine, Bovine, and Human Embryos [PDF]

open access: yes, 2016
The use of preimplantation genetic testing (PGT) in reproductive medicine and animal production has increased significantly in the last few years. Preimplantation genetic testing starts with the collection of a few cells from the embryo and continues ...
Herrera, Carolina
core   +2 more sources

Preimplantation Genetic Testing: A Fundamental Right [PDF]

open access: yes, 2022
Unlike many European countries of similar economic, social, scientific, and political advancement, there is virtually no regulation of preimplantation genetic testing in the United States.
Swann, Julianna S.
core   +1 more source

Preimplantation genetic testing for familial amyloid polyneuropathy

open access: yesReproductive Health, 2022
Background Embryo selection in Familial amyloid polyneuropathy eradicates the disease, but the widespread application of preimplantation genetic testing (PGT) for this monogenic disease still requires greater political and clinical commitment.
Mário Sousa
doaj   +1 more source

Embryo ploidy status classification through computer-assisted morphology assessmentAJOG MFM at a Glance

open access: yesAJOG Global Reports, 2023
BACKGROUND: Preimplantation genetic testing for aneuploidy has been proven to be effective in determining the embryo's chromosomal or ploidy status. The test requires a biopsy of embryonic cells on day 3, 5, or 6 from which complete information on the ...
Gunawan Bondan Danardono, SKom, BEng   +8 more
doaj   +1 more source

Prenatal mucopolysaccharidosis VII: A novel pathogenic variant identified in GUSB gene

open access: yesClinical Case Reports, 2021
Clinical exome sequencing is a powerful approach to overcome the wide clinical and genetic heterogeneity of mucopolysaccharidosis. These data could be useful for prenatal diagnosis of MPS VII, genetic counseling, and preimplantation genetic testing.
Antonio Miguel Poyatos‐Andújar   +6 more
doaj   +1 more source

Pre-implantation Genetic Testing for Aneuploidy (PGT-A)

open access: yesThai Journal of Obstetrics and Gynaecology, 2020
Preimplantation genetic diagnosis (PGD) or embryo selection was first performed in 1989 using PCR for gender selection to avoid X-linked recessive disorder. However, there was a misdiagnosis due to allele drop out (ADO). Therefore, fluorescent in situ
Wirawit Piyamongkol
doaj   +1 more source

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