A systematic review of reported cases of pachyonychia congenita tarda
Author:
Affiliation:
1. Department of Dermatology Liverpool Hospital Sydney NSW Australia
2. University of New South Wales Sydney NSW Australia
3. Ingham Institute of Applied Medical Research Liverpool, Sydney NSW Australia
Publisher
Wiley
Subject
Dermatology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/ced.13980
Reference17 articles.
1. Pachyonychia Congenita Tarda
2. Delayed-onset pachyonychia congenita associated with a novel mutation in the central 2B domain of keratin 16
3. Delayed-onset pachyonychia congenita caused by a novel mutation in the V2 domain of keratin 6b
4. A Novel Mutation in the Second Half of the Keratin 17 1A Domain in a Large Pedigree with Delayed-Onset Pachyonychia Congenita Type 2
5. Novel keratin 16 mutations and protein expression studies in pachyonychia congenita type 1 and focal palmoplantar keratoderma
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1. Corrigendum;Clinical and Experimental Dermatology;2021-09-23
2. Distinctions in the Management, Patient Impact, and Clinical Profiles of Pachyonychia Congenita Subtypes;Skin Appendage Disorders;2021
3. Pachyonychia Congenita;Diseases of the Oral Mucosa;2021
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