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 Printable version |
Compound heterozygosity for the Xeroderma pigmentosum complementation group A gene associated with a mild phenotype |
European Journal of Dermatology. Volume 12, Number 6, 536-9, November - December 2002, Gènes et peau
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 Free Article
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Author(s) : Izumi NEGISHI, Go KATO, Shinichi MORIWAKI, Osamu ISHIKAWA |
Summary : We describe a case of a 7-year-old boy diagnosed as xeroderma pigmentosum complementation group A (XPA). Severe photosensitivity developed at 5 months after birth, and at a visit to our hospital at the age of five years, multiple brownish freckles were present on the face. XPA complementing (XPAC) gene compensated the ability of DNA repair after UV-irradiation of the fibroblasts. PCR-RFLP and DNA sequencing analyses revealed compound heterozygosity for a splicing mutation (IV3 -1G => C) at the splicing acceptor site of intron 3 and a nonsense mutation (Arg228 => stop) in exon 6. The former mutation can be detected by a restriction enzyme Alw NI and the latter detected by Hph I. Neither obvious neurological symptoms nor malignant skin tumors were noted. This genotype is associated with milder clinical symptoms than homozygosity for the IV3 -1G => C mutation. |
Keywords : compound heterozygote, Xeroderma pigmentosum group A, genotype-phenotype correlation. |
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