Genetic counseling for pre-implantation genetic testing of monogenic disorders (PGT-M) [PDF]
Pre-implantation genetic testing (PGT) is a vital tool in preventing chromosomal aneuploidies and other genetic disorders including those that are monogenic in origin. It is performed on embryos created by intracytoplasmic sperm injection (ICSI). Genetic
Firuza Parikh +6 more
doaj +2 more sources
Simultaneous detection of genomic imbalance in patients receiving preimplantation genetic testing for monogenic diseases (PGT-M) [PDF]
Background: Preimplantation genetic test for monogenic disorders (PGT-M) has been used to select genetic disease-free embryos for implantation during in vitro fertilization (IVF) treatment.
Lin Yang +26 more
doaj +2 more sources
Outcomes and the effect of PGT-M in women with hormone-related hereditary tumor syndrome [PDF]
PurposeTo review the outcome of PGT-M in hormone-related hereditary tumor syndrome and evaluate the effect of ovarian induction on tumor growth in those patients.MethodsMedical records of PGT-M were retrospectively analyzed in patients with hormone ...
Dingran Wang +7 more
doaj +2 more sources
The Role of Preimplantation Genetic Testing for Monogenic Disorders (PGT-M) in Hemoglobinopathy Management—Techniques, Accuracy, and the Balancing of Benefits and Drawbacks [PDF]
Preimplantation genetic testing for monogenic disorders (PGT-M) is a powerful tool for identifying genetic disorders prior to gestation. For hemoglobinopathies like thalassemias and sickle cell disease, PGT-M offers a preventative strategy to ensure that
Rasrawee Chantrasiri +5 more
doaj +2 more sources
Preimplantation genetic testing for aneuploidies (PGT-A) and PGT for monogenic disorders (PGT-M) have currently been used widely, aiming to improve IVF outcomes.
Hsin-Fu Chen, Hong-Nerng Ho
exaly +3 more sources
Background and objectives: Preimplantation genetic testing (PGT) offers patients the possibility of having a healthy baby free of chromosomal or genetic disorders.
Alexandra Papadopoulou +2 more
exaly +3 more sources
Case Report: Preventing X-linked retinoschisis transmission via MARSALA-based PGT-M [PDF]
X-linked retinoschisis (XLRS) is an X-linked recessive inherited retinal disease caused by mutations in the RS1 gene. This case report describes the successful application of preimplantation genetic testing for monogenic diseases (PGT-M) to prevent the ...
Jieliang Li +9 more
doaj +2 more sources
Factors associated with de novo aneuploidy across different preimplantation genetic testing cycles: a retrospective cohort study [PDF]
ObjectivePrevious studies on factors influencing embryonic aneuploidy have produced inconsistent results. This study aimed to identify predictors of de novo aneuploidy in distinct patients undergoing preimplantation genetic testing for structural ...
Hongfang Liu +11 more
doaj +2 more sources
Development of pre-implantation genetic testing protocol for monogenic disorders (PGT-M) of Hb H disease [PDF]
Hb H disease is the most severe form of α-thalassemia compatible with post-natal life. Compound heterozygous α0-thalassemia− SEA deletion/α+-thalassemia− 3.7kb deletion is the commonest cause of Hb H disease in Thailand.
Pannarai Somboonchai +5 more
doaj +2 more sources
Objective: To assess whether primary care specialists’ demographics, specialty, and knowledge of preimplantation genetic testing for monogenic disorders (PGT-M) influence their practice patterns. Design: Cross-sectional survey study.
Sarah Capelouto, M.D. +5 more
doaj +1 more source

