| Literature DB >> 25454817 |
Michael Karass1, Mina M Naguib, Nancy Elawabdeh, Caitlin A Cundiff, Jenna Thomason, Charlotte Katherine Steelman, Ryan Cone, Ann Schwenkter, Caroline Jordan, Bahig M Shehata.
Abstract
Xeroderma pigmentosum (XP) is a rare autosomal recessive disorder characterized by hypersensitivity of the skin and eyes to UV-radiation as a result of a defect in one of eight genes. Seven genes (XPA-XPG) have a defect in Nucletoide Excision Repair (NER), while the eighth gene XPV has a defect in polymerase η, which is responsible for replication of UV-damaged DNA to produce corrected daughter strands. We present the varied clinical courses of three African-American female patients with XP. Additionally, we present a review of the literature that focuses on the various clinical manifestations as well as the genetic and molecular mechanisms underlying this disease.Entities:
Keywords: autosomal recessive; nucleotide excision repair; xeroderma pigmentosum
Mesh:
Year: 2014 PMID: 25454817 DOI: 10.3109/15513815.2014.982336
Source DB: PubMed Journal: Fetal Pediatr Pathol ISSN: 1551-3815 Impact factor: 0.958