Does progressive symmetric erythrokeratoderma exist?
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2133.2004.05965.x/fullpdf
Reference14 articles.
1. Towards a better classification of erythrokeratodermias
2. The Molecular Pathology of Progressive Symmetric Erythrokeratoderma: A Frameshift Mutation in the Loricrin Gene and Perturbations in the Cornified Cell Envelope
3. Loricrin keratoderma: a cause of congenital ichthyosiform erythroderma and collodion baby.
4. Progressive symmetric erythrokeratodermia
5. Generalized Erythematous Plaques
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1. Expanding the clinical phenotype associated with NIPAL4 mutation: Study of a Tunisian consanguineous family with erythrokeratodermia variabilis—Like Autosomal Recessive Congenital Ichthyosis;PLOS ONE;2021-10-20
2. A heterozygous mutation in GJA1 gene in Chinese family with serious erythrokeratodermia variabilis et progressive;Chinese Medical Journal;2019-01-05
3. Dominant De Novo Mutations in GJA1 Cause Erythrokeratodermia Variabilis et Progressiva, without Features of Oculodentodigital Dysplasia;Journal of Investigative Dermatology;2015-06
4. Progressive symmetric erythrokeratoderma having overlapping features with erythrokeratoderma variabilis and lesional hypertrichosis: Is nomenclature "erythrokeratoderma variabilis progressiva" more appropriate?;Indian Journal of Dermatology;2015
5. Érythrokératodermie variable;Annales de Dermatologie et de Vénéréologie;2013-02
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