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Volumn 77, Issue 3, 1997, Pages 225-227
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Keratosis linearis with ichthyosis congenita and sclerosing keratoderma (KLICK-syndrome): A rare, autosomal recessive disorder of keratohyaline formation?
a,d b c |
Author keywords
epidermal differentiation; etretinate; genodermatosis; inborn errors of keratinization
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Indexed keywords
ETRETINATE;
RETINOID;
ADULT;
ARTICLE;
AUTOSOMAL RECESSIVE DISORDER;
CASE REPORT;
CLINICAL FEATURE;
CONGENITAL ICHTHYOSIFORM ERYTHRODERMA;
DISEASE COURSE;
ELECTRON MICROSCOPY;
HISTOLOGY;
HUMAN;
HUMAN TISSUE;
HYPERKERATOSIS;
KERATOSIS PALMOPLANTARIS;
MALE;
ORAL DRUG ADMINISTRATION;
PRIORITY JOURNAL;
SKIN BIOPSY;
ADULT;
HUMANS;
ICHTHYOSIS;
KERATODERMA, PALMOPLANTAR;
KERATOSIS;
MALE;
MICROSCOPY, ELECTRON;
SYNDROME;
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EID: 0030910411
PISSN: 00015555
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
Times cited : (31)
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References (8)
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