Acral peeling skin syndrome: A clinically and genetically heterogeneous disorder

Pediatric Dermatology

Volumn 29, Issue 3, 2012, Pages 258-263

  Pavlovic, Sasha ^a   Krunic, Aleksandar L ^a   Bulj, Tanja K ^a   Medenica, Maria M ^b   Fong, Kenneth ^c   Arita, Ken ^c   McGrath, John A ^c  

^a UNIVERSITY OF ILLINOIS   (United States)

^b UNIVERSITY OF CHICAGO   (United States)

^c KING'S COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ALUMINUM CHLORIDE; LANOLIN ALCOHOL; TRIACYLGLYCEROL; XIPAMIDE;

ACRAL PEELING SKIN SYNDROME; ADULT; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; AUTOSOMAL RECESSIVE INHERITANCE; CASE REPORT; CHROMOSOME 1; CHROMOSOME 10; CHROMOSOME 13; CHROMOSOME 16; CHROMOSOME 6; CHROMOSOME MAP; CONSANGUINITY; ERYTHEMA; FAMILY; FAMILY HISTORY; GENE; GENE MUTATION; GENE SEQUENCE; GENETIC DISORDER; GENETIC SCREENING; GENODERMATOSIS; HOMOZYGOSITY; HUMAN; JORDAN; MALE; MEDICAL HISTORY; PEDIGREE ANALYSIS; PRIORITY JOURNAL; SKIN ABRASION; SKIN PRURITUS; TGM5 GENE;

ADOLESCENT; BASE SEQUENCE; CHROMOSOME MAPPING; CONSANGUINITY; DERMATITIS, EXFOLIATIVE; FEMALE; GENETIC VARIATION; HOMOZYGOTE; HUMANS; JORDAN; MALE; MOLECULAR SEQUENCE DATA; PEDIGREE; PIGMENTATION DISORDERS; TRANSGLUTAMINASES; YOUNG ADULT;

EID: 84861338903     PISSN: 07368046     EISSN: 15251470     Source Type: Journal    
DOI: 10.1111/j.1525-1470.2011.01563.x     Document Type: Article

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