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Novel Variant and a Possible New Founder Effect for Xeroderma Pigmentosum Variant Type in Southeast Brazil: Case
Leonardo Ávila Ferreira1, Mara Sanches Guaragna2, Carlos Eduardo Steiner2
1Dermatology Division, Department of Internal Medicine, School of Medical Sciences, University of Campinas (UNICAMP), Campinas, Brazil.
Case Reports in Dermatology
|August 13, 2026
Summary
Xeroderma pigmentosum variant (XP-V) patients with a novel POLH gene splice site variant developed skin cancers and ocular issues but no neurological symptoms. This suggests a potential founder effect in Brazil.
Area of Science:
- Genetics
- Dermatology
- Ophthalmology
Background:
- Xeroderma pigmentosum (XP) is a group of genodermatoses characterized by autosomal recessive inheritance and increased photosensitivity.
- XP comprises 9 subtypes (A-J) plus a variant (V) type, with some subtypes prone to ocular disease and neurodegeneration.
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