What’s the resolutive surgery for pseudo-ainhum in Vohwinkel syndrome? A case report and review of the literature

Vohwinkel Syndrome, also known as Keratoderma Hereditarium Mutilans, is an extremely rare dominant autosomal keratosis. It typically presents with “starfish” keratoses on the knuckles, palmoplantar keratoderma (PPK), hearing impairment and mutilating digital constriction bands (pseudoainhum) that ca...

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Detalles Bibliográficos
Autores principales: Rovere, Giuseppe, Stramazzo, Leonardo, Cioffi, Alessio, Galvano, Nicolò, Pavan, Davide, Restuccia, Giuseppe, D’Arienzo, Antonio, Capanna, Rodolfo, Maccauro, Giulio, D’Arienzo, Michele, Camarda, Lawrence
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications, Pavia, Italy 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7883105/
https://www.ncbi.nlm.nih.gov/pubmed/33633820
http://dx.doi.org/10.4081/or.2020.8868

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7883105/
https://www.ncbi.nlm.nih.gov/pubmed/33633820
http://dx.doi.org/10.4081/or.2020.8868

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