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About 293 results

ALLMedicine™ Triploidy Center

Research & Reviews  112 results

Non-invasive prenatal screening for fetal triploidy using single nucleotide polymorphis...
https://doi.org/10.1002/pd.6169
Prenatal Diagnosis; Kantor V, Jelsema R et. al.

May 17th, 2022 - An extra haplotype is infrequently encountered in SNP-based non-invasive prenatal testing (NIPT) and is usually attributed to an undetected twin or triploidy. We reviewed a large series to establish relative frequencies of these outcomes and ident...

In vitro fertilization and preimplantation genetic diagnosis outcomes in mosaic Turner'...
https://doi.org/10.1016/j.jogoh.2022.102405
Journal of Gynecology Obstetrics and Human Reproduction; Acet F, Sahin G et. al.

May 16th, 2022 - Patients with mosaic Turner syndrome who have normal phenotype and pubertal development may be diagnosed based on karyotype examination which is performed due to recurrent abortion or recurrent implantation failure; but according to the literature...

Extended survival of a premature infant with a postnatal diagnosis of complete triploidy.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8823055
BMJ Case Reports; Walsh R, Sharma A

Feb 9th, 2022 - Triploidy is a common chromosomal abnormality that usually results in spontaneous abortion. Liveborn infants usually die within hours or days of birth. We present the case of a female infant born at 30 weeks and 5 days of gestation who received a ...

Haplotype-aware inference of human chromosome abnormalities.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8609623
Proceedings of the National Academy of Sciences of the Un... Ariad D, Yan SM et. al.

Nov 14th, 2021 - Extra or missing chromosomes-a phenomenon termed aneuploidy-frequently arise during human meiosis and embryonic mitosis and are the leading cause of pregnancy loss, including in the context of in vitro fertilization (IVF). While meiotic aneuploidi...

Effect of preexamination conditions in a centralized-testing model of non-invasive pren...
https://doi.org/10.1515/cclm-2021-0652
Clinical Chemistry and Laboratory Medicine; Fibke C, Giroux S et. al.

Nov 12th, 2021 - Non-invasive prenatal testing requires the presence of fetal DNA in maternal plasma. Understanding how preexamination conditions affect the integrity of cell-free DNA (cfDNA) and fetal fraction (FF) are a prerequisite for test implementation. Ther...

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Clinicaltrials.gov  1 results

Feasibility of Risk-Adapted Therapy in Young Adult Acute Lymphoblastic Leukemia: a Multicenter Trial
https://clinicaltrials.gov/ct2/show/NCT00222027

Jan 7th, 2009 - 1) baseline (BL) : WBC30G/L in B-lineage, CNS involvement, MLL-AF4 and E2A-PBX fusions, haploidy/near-triploidy; 2) early response (ER) : corticoresistance after prophase (CsR), chemoresistance at Day 8 (ChR); all CsR and/or ChR patients are plann...

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News  4 results

Atrioventricular Block Common in Children With Multisystem Inflammatory Syndrome
https://www.staging.medscape.com/viewarticle/940084

Nov 2nd, 2020 - NEW YORK (Reuters Health) - Atrioventricular block (AVB) occurs in about one of five children with multisystem inflammatory syndrome (MIS-C) following SARS-CoV-2 infection, according to a new study. Initial reports from Europe on the features of M...

Atrioventricular Block Common in Children With Multisystem Inflammatory Syndrome
https://www.medscape.com/viewarticle/940084

Nov 2nd, 2020 - NEW YORK (Reuters Health) - Atrioventricular block (AVB) occurs in about one of five children with multisystem inflammatory syndrome (MIS-C) following SARS-CoV-2 infection, according to a new study. Initial reports from Europe on the features of M...

Placental Signs May Augur Autism
https://www.medpagetoday.com/genetics/generalgenetics/3638

Jun 27th, 2006 - Action Points Explain to interested patients that this small study suggests that placental tissues may contain findings associated with the presence of autism spectrum disorders in children, but that the findings need to be replicated in larger, m...

Ultrasonographic Soft Markers of Aneuploidy in Second Trimester: Are We Lost?
https://www.medscape.com/viewarticle/518149

Abstract Chromosomal abnormalities occur in 0.1% to 0.2% of live births, and the most common clinically significant aneuploidy among live-born infants is Down syndrome (trisomy 21). Other sonographically detectable aneuploidies include trisomy 13,...

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