Unusual Disease-Progression in Two Siblings With Xeroderma Pigmentosum Group G
Elena Botta1, Heather Fawcett2, Donata Orioli1
1Institute of Molecular Genetics-CNR, Pavia, Italy.
Clinical Genetics
|January 3, 2026
Summary
Protein truncation mutations in the Xeroderma Pigmentosum Group D (XPG) nuclease gene lead to severe disease. However, two siblings with splicing mutations causing in-frame deletions showed a milder clinical phenotype, suggesting a genotype-phenotype correlation.
Area of Science:
- Molecular biology
- Genetics
- Clinical medicine
Background:
- Mutations in the Xeroderma Pigmentosum Group D (XPG) nuclease gene are associated with severe clinical phenotypes.
- XPG nuclease plays a critical role in DNA repair pathways.
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