Altered lameliar body secretion and stratum corneum membrane structure in netherton syndrome: Differentiation from other infantile erythrodermas and pathogenic implications

Archives of Dermatology

Volumn 135, Issue 7, 1999, Pages 823-832

  Fartasch, Manigé ^a   Williams, Mary L ^b,c   Elias, Peter M ^b,c  

^a UNIVERSITY OF ERLANGEN NUREMBERG   (Germany)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c SAN FRANCISCO VETERANS AFFAIRS MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CELL SECRETION; CLINICAL ARTICLE; CONGENITAL ICHTHYOSIFORM ERYTHRODERMA; CONTROLLED STUDY; DIFFERENTIAL DIAGNOSIS; DISEASE MARKER; ERYTHRODERMA; FAILURE TO THRIVE; FEMALE; HUMAN; HUMAN TISSUE; HYPERNATREMIA; INFANT; LAMELLAR BODY; MALE; MEMBRANE STRUCTURE; NETHERTON DISEASE; PARAKERATOSIS; PRESCHOOL CHILD; PRIORITY JOURNAL; PSORIASIS; STRATUM CORNEUM; CONGENITAL MALFORMATION; ELECTRON MICROSCOPY; HAIR; ICHTHYOSIS; IMMEDIATE TYPE HYPERSENSITIVITY; PATHOLOGY; SECRETION; SKIN; SYNDROME;

CHILD, PRESCHOOL; FEMALE; HAIR; HUMANS; HYPERSENSITIVITY, IMMEDIATE; ICHTHYOSIS; INFANT; MALE; MICROSCOPY, ELECTRON; SKIN; SYNDROME;

EID: 0032588114     PISSN: 0003987X     EISSN: None     Source Type: Journal    
DOI: 10.1001/archderm.135.7.823     Document Type: Article

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