A case of type 1 segmental Darier disease showing widespread Blaschkoid skin lesions with p.P160L mutation in ATP2A2
Author:
Affiliation:
1. Department of Dermatology Teikyo University School of Medicine Tokyo Japan
2. Department of Dermatology Keio University School of Medicine Shinjuku Japan
Publisher
Wiley
Subject
Infectious Diseases,Dermatology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/jdv.16506
Reference10 articles.
1. Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease
2. Darier Disease with Paired Segmental Manifestation of Either Excessive or Absent Involvement: A Further Step in the Concept of Twin Spotting
3. The categories of cutaneous mosaicism: A proposed classification
4. P160L Mutation in the Ca2+ ATPase 2A Domain in a Patient with Severe Darier Disease
5. Darier disease in Slovenia: spectrum of ATP2A2 mutations and relation to patients’ phenotypes
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1. Mosaicism for ATP2A2 Mutation and Mutant Allelic Fractions Detected by Droplet Digital PCR in Simple Segmental Darier Disease;Acta Dermato-Venereologica;2023-07-13
2. Association of Somatic ATP2A2 Damaging Variants With Grover Disease;JAMA Dermatology;2023-07-01
3. Case of type 1 segmental Darier's disease with a novel mosaic mutation in the ATP2A2 gene;The Journal of Dermatology;2023-03-08
4. Acné hemicraneal y lesiones lineales en el hemicuerpo: una rara presentación de la enfermedad de Darier segmentaria;Piel;2021-08
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