Ultrastructural features resembling those of harlequin ichthyosis in patients with severe congenital ichthyosiform erythroderma

British Journal of Dermatology

Volumn 145, Issue 3, 2001, Pages 480-483

  Virolainen, E ^a,c   Niemi, K M ^a,c   Ganemo A ^d   Kere, J ^b   Vahlquist, A ^d   Saarialho Kere, Ulpu ^a,c  

^a UNIVERSITY OF HELSINKI   (Finland)

^b UNIVERSITY OF HELSINKI   (Finland)

^c HELSINKI UNIVERSITY CENTRAL HOSPITAL   (Finland)

^d UPPSALA UNIVERSITY HOSPITAL   (Sweden)

Author keywords

Autosomal recessive congenital ichthyosis; Electron microscopy; Harlequin ichthyosis; Lamellar granules; Lamellar ichthyosis; Non bullous congenital ichthyosiform erythroderma

Indexed keywords

KERATOHYALIN; PROTEIN GLUTAMINE GAMMA GLUTAMYLTRANSFERASE;

ADOLESCENT; ADULT; ALOPECIA; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CELL ORGANELLE; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; CONGENITAL ICHTHYOSIFORM ERYTHRODERMA; DISEASE CLASSIFICATION; DISEASE SEVERITY; ECTROPION; ELECTRON MICROSCOPY; EPIDERMIS CELL; FEMALE; FINGER MALFORMATION; GENE MUTATION; HARLEQUIN ICHTHYOSIS; HUMAN; LAMELLAR BODY; MALE; PHENOTYPE; PRIORITY JOURNAL; SCALP; SCANDINAVIA; TOE MALFORMATION; ULTRASTRUCTURE;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; FEMALE; HUMANS; ICHTHYOSIFORM ERYTHRODERMA, CONGENITAL; ICHTHYOSIS, LAMELLAR; MALE; MICROSCOPY, ELECTRON; MIDDLE AGED; SKIN;

EID: 0034799588     PISSN: 00070963     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2133.2001.04401.x     Document Type: Article

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