Inflammatory peeling skin syndrome caused by homozygous genomic deletion in the PSORS1 region encompassing the CDSN gene

Experimental Dermatology

Volumn 23, Issue 1, 2014, Pages 60-63

  Ishida Yamamoto, Akemi ^a   Furio, Laetitia ^b   Igawa, Satomi ^a   Honma, Masaru ^a   Tron, Elodie ^c   Malan, Valerie ^c   Murakami, Masamoto ^a   Hovnanian, Alain ^b,c  

^a ASAHIKAWA MEDICAL COLLEGE   (Japan)

^b IMAGINE INSTITUTE   (France)

^c HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

Corneodesmosin; Peeling skin syndrome; PSORS1

Indexed keywords

CORNEODESMOSIN; PROTEIN; UNCLASSIFIED DRUG;

ADOLESCENT; CASE REPORT; EXON; GENE DELETION; GENE MUTATION; GENODERMATOSIS; HAPLOTYPE; HUMAN; IMMUNOHISTOCHEMISTRY; JAPANESE; LETTER; MALE; MICROADENOMA; PEELING SKIN SYNDROME; POLYMERASE CHAIN REACTION; PROTEIN EXPRESSION; RARE DISEASE; SKIN ABRASION;

CORNEODESMOSIN; PEELING SKIN SYNDROME; PSORS1;

ADOLESCENT; ASIAN CONTINENTAL ANCESTRY GROUP; CHROMOSOMES, HUMAN, PAIR 6; DERMATITIS, EXFOLIATIVE; FEMALE; GENE DELETION; GLYCOPROTEINS; HAPLOTYPES; HOMOZYGOTE; HUMANS; JAPAN; MALE; PEDIGREE; SKIN DISEASES, GENETIC;

EID: 84891369484     PISSN: 09066705     EISSN: 16000625     Source Type: Journal    
DOI: 10.1111/exd.12292     Document Type: Letter

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