A unique pattern of dyskeratosis characterizes epidermolytic hyperkeratosis and epidermolytic palmoplantar keratoderma

American Journal of Dermatopathology

Volumn 30, Issue 2, 2008, Pages 101-105

  Bergman, Reuven ^a   Khamaysi, Ziad ^a   Sprecher, Eli ^a  

^a TECHNION ISRAEL INSTITUTE OF TECHNOLOGY   (Israel)

Author keywords

Dyskeratosis; Epidermolytic; Histology; Keratin; Keratoderma

Indexed keywords

KERATIN;

ADOLESCENT; ADULT; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CELL AGGREGATION; CELL INCLUSION; CELL NUCLEUS; CLINICAL FEATURE; CYTOPLASM; DARIER DISEASE; DYSKERATOSIS; EOSINOPHIL; EPIDERMOLYTIC HYPERKERATOSIS; EPIDERMOLYTIC PALMOPLANTAR KERATODERMA; FEMALE; GENE; GENE MUTATION; GENODERMATOSIS; HISTOLOGY; HUMAN; ICHTHYOSIS HYSTRIX OF CURTH MACKLIN; KERATINOCYTE; KERATODERMA; KRT1 GENE; KRT9 GENE; MALE; PRIORITY JOURNAL; SCHOOL CHILD; SKIN BIOPSY; TONOFILAMENT; ULTRASTRUCTURE; VOLAR PLATE;

ADOLESCENT; ADULT; BIOPSY, NEEDLE; CHILD; DNA MUTATIONAL ANALYSIS; FEMALE; HUMANS; HYPERKERATOSIS, EPIDERMOLYTIC; IMMUNOHISTOCHEMISTRY; KERATIN-1; KERATINS; KERATODERMA, PALMOPLANTAR, EPIDERMOLYTIC; MALE; MICROSCOPY, ELECTRON; MUTATION, MISSENSE; SAMPLING STUDIES; SENSITIVITY AND SPECIFICITY; SKIN;

EID: 41149130170     PISSN: 01931091     EISSN: None     Source Type: Journal    
DOI: 10.1097/DAD.0b013e3181614898     Document Type: Article

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