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Updated: Apr 12, 2026

Single-Molecule Fluorescence Visualization of DNA Polymerase Dynamics at G-Quadruplexes
Published on: April 4, 2025
A patient with polymerase E1 deficiency (POLE1): clinical features and overlap with DNA breakage/instability
Isabelle Thiffault1,2, Carol Saunders3,4,5, Janda Jenkins6,7,8
1Center for Pediatric Genomic Medicine, Children's Mercy Hospital, Kansas City, MO, 64108, USA. ithiffault@cmh.edu.
Background:
Chromosome instability syndromes are a group of inherited conditions associated with chromosomal instability and breakage, often leading to immunodeficiency, growth retardation and increased risk of malignancy.
Case Presentation:
We performed exome sequencing on a girl with a suspected chromosome instability syndrome that manifested as growth retardation, microcephaly, developmental delay, dysmorphic features, poikiloderma, immune deficiency with pancytopenia, and myelodysplasia. She was homozygous for a previously reported splice variant, c.4444 + 3A > G in the POLE1 gene, which encodes the catalytic subunit of DNA polymerase E.
Conclusion:
This is the second family with POLE1-deficency, with the affected individual demonstrating a more severe phenotype than previously described.
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