Poikiloderma a varied presentation - Huriez syndrome

Huriez syndrome is a rare autosomal dominant genodermatosis characterized by the triad of congenital scleroatrophy of the distal extremities, palmoplantar keratoderma (PPK) and hypoplastic nails. We report the case of a 25 year old male, with nonfamilial Huriez syndrome.

Detalles Bibliográficos
Autores principales: Kharge, Priyadarshini, Fernendes, Carol, Jairath, Vijayeeta, Mohan, Madan, Chandra, Suresh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4314883/
https://www.ncbi.nlm.nih.gov/pubmed/25657913
http://dx.doi.org/10.4103/2229-5178.148929

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4314883/
https://www.ncbi.nlm.nih.gov/pubmed/25657913
http://dx.doi.org/10.4103/2229-5178.148929

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