Dual clinical features of fine and rough scales seen in a combined ichthyosis vulgaris and X‐linked recessive ichthyosis patient with atopic dermatitis
Author:
Affiliation:
1. Department of Dermatology Nagoya University Graduate School of Medicine Nagoya Japan
2. Department of Dermatology and Plastic Surgery Akita University Graduate School of Medicine Akita Japan
Funder
Japan Agency for Medical Research and Development
Japan Society for the Promotion of Science
Publisher
Wiley
Subject
Dermatology,General Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/1346-8138.16968
Reference5 articles.
1. Unique mutations in the filaggrin gene in Japanese patients with ichthyosis vulgaris and atopic dermatitis
2. The phenotype spectrum of X-linked ichthyosis identified by chromosomal microarray
3. Increased Prevalence of Filaggrin Deficiency in 51 Patients with Recessive X-Linked Ichthyosis Presenting for Dermatological Examination
4. Exacerbation of X-linked ichthyosis phenotype in a female by inheritance of filaggrin and steroid sulfatase mutations
5. Steroid sulfatase and filaggrin mutations in a boy with severe ichthyosis, elevated serum IgE level and moyamoya syndrome
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