Application of genetic scissoring in the management of genetically related diseases

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CRISPR technology enables precise genome editing, allowing targeted modification of DNA sequences.
Applications of CRISPR include treating genetic diseases like sickle cell anemia and cystic fibrosis.
The technology utilizes the cas9 endonuclease to introduce site-specific cuts in the genome for gene therapy.
Ethical challenges remain with CRISPR, particularly regarding unintended genetic modifications and access to therapy.

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CRISPR technology demonstrates potential in targeting monogenic and polygenic disorders, suggesting new gene therapies.

Ogunlakin et al. (2025) studied this question.

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