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Related Concept Videos

Teratogenicity01:07

Teratogenicity

The ability of a drug to produce structural deformations and functional abnormalities in the developing embryo or the fetus is called teratogenicity, and the drug producing this effect is known as a teratogen. Teratogenic effects include stillbirth, miscarriage, intrauterine growth restriction, and neurocognitive delay. A teratogen may affect the embryo at different stages of development, which is important in determining the type and extent of the damage. During blastocyst formation, the early...
Meiosis vs. Mitosis02:57

Meiosis vs. Mitosis

Cell division is necessary for growth and reproduction in organisms. Mitosis aids cell growth and development by dividing somatic cells. In contrast, meiosis causes the division of germ cells and plays an essential role in sexual reproduction. Due to their unique functional requirements, mitosis and meiosis differ from each other in multiple aspects.
Before the start of mitosis and meiosis I, the cell synthesizes DNA, resulting in two homologous copies of each chromosome. DNA synthesis is...
Nondisjunction01:29

Nondisjunction

During meiosis, chromosomes occasionally separate improperly. This occurs due to failure of homologous chromosome separation during meiosis I or failed sister chromatid separation during meiosis II. In some species, notably plants, nondisjunction can result in an organism with an entire additional set of chromosomes, which is called polyploidy. In humans, nondisjunction can occur during male or female gametogenesis and the resulting gametes possess one too many or one too few chromosomes.
Nondisjunction01:21

Nondisjunction

Nondisjunction is the failure of homologous chromosomes or sister chromatids to separate correctly and move to the opposite poles of the cells. This produces daughter cells with abnormal chromosome numbers.  Nondisjunction is common during anaphase I or anaphase II of meiosis.  Mutations in synaptonemal complex proteins that attach homologous chromosomes increase the chances of nondisjunction in anaphase I of meiosis I. In contrast, mutations in topoisomerases and condensins that hold sister...
Oogenesis02:07

Oogenesis

In human women, oogenesis produces one mature egg cell or ovum for every precursor cell that enters meiosis. This process differs in two unique ways from the equivalent procedure of spermatogenesis in males. First, meiotic divisions during oogenesis are asymmetric, meaning that a large oocyte (containing most of the cytoplasm) and minor polar body are produced as a result of meiosis I, and again following meiosis II. Since only oocytes will go on to form embryos if fertilized, this unequal...
Reproductive Cloning01:27

Reproductive Cloning

Reproductive cloning is the process of producing a genetically identical copy—a clone—of an entire organism. While clones can be produced by splitting an early embryo—similar to what happens naturally with identical twins—cloning of adult animals is usually done by a process called somatic cell nuclear transfer (SCNT).
Somatic Cell Nuclear Transfer
In SCNT, an egg cell is taken from an animal and its nucleus is removed, creating an enucleated egg. Then a somatic cell—any cell that is not a sex...

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Monitoring Blood Glucose in Mouse Offspring After Intracytoplasmic Sperm Injection
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Is assisted reproduction associated with abnormal placentation?

Jolly Joy1, Caroline Gannon, Neil McClure

  • 1Obstetrics and Gynaecology, Mulhouse Building, Queen's University Belfast, Grosvenor Road, Belfast, BT12 6BJ, Northern Ireland. jolly.joy@belfastrust.hscni.net

Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society
|May 19, 2012
PubMed
Summary

Artificial reproductive technologies (ART) and infertility impact placental health. ART pregnancies showed thicker placentas and more hematomas, potentially increasing perinatal risks.

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Area of Science:

  • Reproductive Medicine
  • Perinatology
  • Pathology

Background:

  • Artificial reproductive technologies (ART) and prolonged infertility are linked to pregnancy complications.
  • The role of placental dysfunction in these complications remains unclear.
  • Histological placental discrepancies may explain observed variances.

Purpose of the Study:

  • To compare placental histopathology in singleton pregnancies conceived via ART, spontaneous conception, and following untreated infertility (>1 year).

Main Methods:

  • Single pathologist examined placentae from 89 women (ART=33, infertility=17, control=39).
  • Exclusion criteria included smoking, medical history, and uterine anomalies.
  • Statistical analysis used ANOVA and chi-square tests.

Main Results:

  • ART placentas were significantly thicker than spontaneous conception placentas (P=0.02).
  • ART placentas had a higher incidence of hematomas (P=0.04).
  • No significant differences in placental shape, cord insertion, or microscopic lesions were found between groups.

Conclusions:

  • Placentas from ART pregnancies exhibit increased thickness and hematoma incidence.
  • These placental changes may contribute to increased perinatal risks.
  • Further research is needed to fully understand ART-related placental pathology.