Collodion baby and loricrin keratoderma: a case report and mutation analysis
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2230.2012.04426.x/fullpdf
Reference10 articles.
1. Towards characterization of palmoplantar keratoderma caused by gain-of-function mutation in loricrin: analysis of a family and review of the literature;Gedicke;Br J Dermatol,2006
2. Loricrin keratoderma: a novel disease entity characterized by nuclear accumulation of mutant loricrin;Ishida-Yamamoto;J Dermatol Sci,2003
3. A novel c.545-546insG mutation in the loricrin gene correlates with a heterogeneous phenotype of loricrin keratoderma;Song;Br J Dermatol,2008
4. Loricrin mutation in Vohwinkel’s keratoderma is unique to the variant with ichthyosis;Korge;J Invest Dermatol,1997
5. A molecular defect in loricrin, the major component of the cornified cell envelope, underlies Vohwinkel’s syndrome;Maestrini;Nat Genet,1996
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1. Collodion Baby Progressing to Camisa Syndrome: Case Report and Review of Literature in Asian Population;Indian Journal of Postgraduate Dermatology;2024-04-23
2. Inherited Disorders of Cornification;Rook's Textbook of Dermatology;2024-03-19
3. Dermatoses of the Neonate;Rook's Textbook of Dermatology;2024-03-19
4. Exploring Pseudoainhum in Camisa syndrome;Clinical Case Reports;2021-10
5. Loricrin keratoderma: description of a novel mutation, systematic review and meta‐analysis between genotypic and phenotypic features;JDDG: Journal der Deutschen Dermatologischen Gesellschaft;2020-08-24
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