Erythrokeratodermia variabilis with erythema gyratum repens-like lesions
Détails
ID Serval
serval:BIB_6F05422741F8
Type
Article: article d'un périodique ou d'un magazine.
Sous-type
Etude de cas (case report): rapporte une observation et la commente brièvement.
Collection
Publications
Institution
Titre
Erythrokeratodermia variabilis with erythema gyratum repens-like lesions
Périodique
Pediatric Dermatology
ISSN
0736-8046 (Print)
Statut éditorial
Publié
Date de publication
08/2002
Volume
19
Numéro
4
Pages
285-92
Notes
Case Reports
Journal Article --- Old month value: Jul-Aug
Journal Article --- Old month value: Jul-Aug
Résumé
A large pedigree with erythrokeratodermia variabilis (EKV) and erythema gyratum repens-like lesions is described. Clinical, laboratory, and histologic findings of this family are presented. The differential diagnoses of the following dermatoses with an erythematous and a hyperkeratotic component are discussed: erythrokeratodermia variabilis (Mendes da Costa), progressive symmetric erythrokeratoderma (Gottron), loricrin keratoderma, erythrokeratoderma en cocardes (Degos), Netherton syndrome, keratitis-ichthyosis-deafness (KID) syndrome, erythrokeratolysis hiemalis (Oudtshoorn disease), and nonbullous congenital ichthyosiform erythroderma.
Mots-clé
Adult
Aged
Biopsy, Needle
Child
Erythema/genetics/pathology
Female
*Genetic Predisposition to Disease
Heterozygote
Humans
Hyperkeratosis, Epidermolytic/*genetics/*pathology
Ichthyosiform Erythroderma, Congenital/genetics/pathology
Immunohistochemistry
Infant
Infant, Newborn
Israel
Male
Middle Aged
Pedigree
Prognosis
Sampling Studies
Severity of Illness Index
Skin Diseases, Genetic/diagnosis
Pubmed
Web of science
Création de la notice
25/01/2008 17:35
Dernière modification de la notice
20/08/2019 15:28