Clinical and genetic characteristics of xeroderma pigmentosum in Nepal.

Date publication

mai 2018

Journal

Journal of the European Academy of Dermatology and Venereology : JEADV

Auteurs

Membres identifiés du Cancéropôle Est :
Pr LEBRE Anne-Sophie

Tous les auteurs :
Espi P, Parajuli S, Benfodda M, Lebre AS, Paudel U, Grange A, Grybek V, Grange T, Soufir N, Grange F

Lien Pubmed

https://www.ncbi.nlm.nih.gov/pubmed/29178624

Résumé

Little is known about xeroderma pigmentosum (XP) in Himalayan countries.

Mots clés

Adolescent, Adult, Carcinoma, Basal Cell, etiology, Carcinoma, Squamous Cell, etiology, Child, Child, Preschool, DNA Mutational Analysis, DNA-Binding Proteins, genetics, Eye Neoplasms, etiology, Female, Heterozygote, High-Throughput Nucleotide Sequencing, Homozygote, Humans, Infant, Keratosis, Actinic, etiology, Male, Mutation, Neoplasms, Multiple Primary, etiology, Nepal, Phenotype, Pilot Projects, Prospective Studies, Receptor, Melanocortin, Type 1, genetics, Skin Neoplasms, etiology, Xeroderma Pigmentosum, complications, Xeroderma Pigmentosum Group A Protein, genetics, Xeroderma Pigmentosum Group D Protein, genetics, Young Adult

Référence

J Eur Acad Dermatol Venereol. 2018 May;32(5):832-839