Related Experiment Video
Updated: Mar 29, 2026

09:03
Semiconductor Sequencing for Preimplantation Genetic Testing for Aneuploidy
Published on: August 25, 2019
10.0K
Live birth resulting from a conjoined oocyte confirmed as euploid using array CGH: a case report.
Lisa Cummins1, Juliette Koch1, Suha Kilani1
1IVF Australia, Level 1, 225 Maroubra Rd, Maroubra, NSW 2035, Australia.
Reproductive Biomedicine Online
|November 26, 2015
Summary
Conjoined oocytes, rare in IVF, can lead to successful pregnancy. This case reports the first pregnancy achieved from a conjoined oocyte, resulting in a healthy baby girl.
Area of Science:
- Reproductive Medicine
- In Vitro Fertilization (IVF)
- Embryology
Background:
- Conjoined oocytes, characterized by two oocytes within a single zona pellucida or fused zonally, are rare in clinical IVF.
- Limited data exists on their significance and developmental potential, often leading to their discard without fertilization attempts.
Observation:
- A conjoined oocyte was identified and processed for IVF.
- The germinal vesicle was removed on day 3, and the resulting embryo was genetically screened.
- A single embryo derived from the conjoined oocyte was transferred.
Findings:
- The embryo developed to the blastocyst stage.
- A clinical pregnancy was confirmed with a gestational sac and fetal heartbeat.
- A healthy baby girl was delivered at 37 weeks' gestation following Caesarean section.
Implications:
- This case demonstrates the potential viability of embryos derived from conjoined oocytes.
- It suggests that conjoined oocytes may not necessarily be non-viable and warrant further investigation.
- This finding could impact laboratory protocols regarding the handling and assessment of conjoined oocytes in IVF.
Related Concept Videos
Nondisjunction
83.5K
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.
83.5K
Nondisjunction
5.7K
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...
5.7K
Nondisjunction
9.9K
9.9K
Crossing Over
174.2K
Unlike mitosis, meiosis aims for genetic diversity in its creation of haploid gametes. Dividing germ cells first begin this process in prophase I, where each chromosome—replicated in S phase—is now composed of two sister chromatids (identical copies) joined centrally.
The homologous pairs of sister chromosomes—one from the maternal and one from the paternal genome—then begin to align alongside each other lengthwise, matching corresponding DNA positions in a process...
The homologous pairs of sister chromosomes—one from the maternal and one from the paternal genome—then begin to align alongside each other lengthwise, matching corresponding DNA positions in a process...
174.2K

