Clinico-epidemiological features of congenital nonbullous ichthyosiform erythroderma in the eastern province of Saudi Arabia
Author:
Publisher
Wiley
Subject
Infectious Diseases,Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1468-3083.2004.01042.x/fullpdf
Reference23 articles.
1. A mother and two children with nonbullous congenital ichthyosiform erythroderma
2. Inherited ichthyoses
3. Lipoxygenase-3 (ALOXE3) and 12(R)-lipoxygenase (ALOX12B) are mutated in non-bullous congenital ichthyosiform erythroderma (NCIE) linked to chromosome 17p13.1
4. Splice-site mutation in TGM1 in congenital recessive ichthyosis in American families: molecular, genetic, genealogic, and clinical studies
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1. Congenital ichthyosiform erythroderma: A rare neonatal dermatoses responding to acitretin;Indian Journal of Pharmacology;2019
2. Inherited Ichthyoses;Pigmented Ethnic Skin and Imported Dermatoses;2018
3. Prevalence of inherited ichthyosis in France: a study using capture-recapture method;Orphanet Journal of Rare Diseases;2014
4. Dermatology Research in Saudi Arabia: Challenges and Hopes;Journal of the Saudi Society of Dermatology & Dermatologic Surgery;2012-07
5. 9 Disorders of epidermal maturation and keratinization;Weedon's Skin Pathology;2010
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