September 10, 2025Vavilov Journal of Genetics and BreedingOpen Access

Familial translocation between chromosomes 3 and 10: meiotic segregation, diagnostics and clinical features of chromosomal

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The study identifies a familial translocation that increases the risk of intellectual disabilities in affected individuals.
Molecular karyotyping clarified breakpoints associated with the translocation, confirming specific chromosomal imbalances.
The proband showed severe cognitive and developmental issues, whereas other family members were carriers without symptoms.
Understanding the mechanisms of chromosomal rearrangements may provide insights into reducing chromosomal pathology risks.

Authors

AVAlexandra V. VozilovaRegional Clinical Hospital No 4 ATA. S. TarasovaRegional Clinical Hospital No 4 EIEvgeny Anatolyevich IvanovV. N. Karazin Kharkiv National University

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Implication

Case study reports meiotic segregation issues and clinical features in a family with chromosomal translocations, indicating increased risk for abnormalities.

Cite This Study

Возилова et al. (2025) studied this question.

synapsesocial.com/papers/68c23bd7b210217d64786de3 https://doi.org/10.18699/vjgb-25-72

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Implication

Case study reports meiotic segregation issues and clinical features in a family with chromosomal translocations, indicating increased risk for abnormalities.

Familial translocation between chromosomes 3 and 10: meiotic segregation, diagnostics and clinical features of chromosomal

Key Points

Discussion

Implication

Cite This Study

Familial translocation between chromosomes 3 and 10: meiotic segregation, diagnostics and clinical features of chromosomal

Key Points

Discussion

Implication

Cite This Study

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