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Related Concept Videos

Meiosis II01:57

Meiosis II

Meiosis II is the second and final stage of meiosis. It relies on the haploid cells produced during meiosis I, each of which contain only 23 chromosomes—one from each homologous initial pair. Importantly, each chromosome in these cells is composed of two joined copies, and when these cells enter meiosis II, the goal is to separate such sister chromatids using the same microtubule-based network employed in other division processes. The result of meiosis II is two haploid cells, each containing...
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In vitro fertilization (IVF) is a form of assisted reproductive technology where an egg is fertilized with sperm in a controlled laboratory environment before transferring the resulting embryo into the uterus. This process is designed to help individuals and couples experiencing difficulties conceiving.
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Meiosis is a carefully orchestrated set of cell divisions, the goal of which—in humans—is to produce haploid sperm or eggs, each containing half the number of chromosomes present in somatic cells elsewhere in the body. Meiosis I is the first such division, and involves several key steps, among them: condensation of replicated chromosomes in diploid cells; the pairing of homologous chromosomes and their exchange of information; and finally, the separation of homologous chromosomes by a...
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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.
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Dysmorphic features in 2-year-old IVF/ICSI offspring.

Jorien Seggers1, Maaike L Haadsma, Arend F Bos

  • 1Dept. Pediatrics, Div. Developmental Neurology, University Medical Center Groningen, The Netherlands.

Early Human Development
|July 17, 2012
PubMed
Summary

Ovarian hyperstimulation and in vitro fertilization (IVF) do not increase dysmorphic features in children. However, longer time to pregnancy (TTP) is linked to a higher risk of abnormalities, suggesting subfertility

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Area of Science:

  • Reproductive Medicine
  • Developmental Biology
  • Pediatrics

Background:

  • Previous studies suggest an increased risk of congenital abnormalities post-IVF/ICSI.
  • Underlying mechanisms for these risks remain unclear.
  • This study investigates factors contributing to dysmorphic features in children conceived via assisted reproductive technologies (ART) and naturally.

Purpose of the Study:

  • To evaluate the impact of ovarian hyperstimulation (OHS), in vitro procedures, and time to pregnancy (TTP) on dysmorphic feature prevalence.
  • To differentiate between minor anomalies and clinically relevant abnormalities.
  • To clarify the role of ART versus underlying subfertility in dysmorphic feature development.

Main Methods:

  • Comparison of singleton births from controlled OHS-IVF/ICSI, modified natural cycle-IVF/ICSI, and naturally conceived subfertile couples.
  • Assessment of dysmorphic features using the Merks et al. method, focusing on minor anomalies.
  • Statistical analysis to determine associations between OHS, IVF/ICSI, TTP, and dysmorphic feature prevalence.

Main Results:

  • No significant difference in dysmorphic feature prevalence was observed between OHS-IVF/ICSI, MNC-IVF/ICSI, and naturally conceived groups.
  • Minor anomalies occurred in approximately 50-54% of children across all groups.
  • A significant association was found between longer TTP (years) and an increased prevalence of abnormalities, particularly clinically relevant ones (aOR=1.22).

Conclusions:

  • Ovarian hyperstimulation and in vitro fertilization procedures are not associated with increased dysmorphic features.
  • The positive association between TTP and clinically relevant abnormalities suggests that underlying subfertility plays a role in their development.
  • Further research is needed to elucidate the specific determinants of subfertility contributing to dysmorphic features.