Netherton syndrome plus atopic dermatitis: Two new genetic mutations in the same patient

A child who comes to our attention for the appearance of erythematous, scaly lesions localized to the upper and lower limbs for 2 months. Histological features suggested ichthyosiform disease and concomitant mutations in the SPINK5 and FLG2 genes confirmed Netherton syndrome with severe atopic manif...

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Detalles Bibliográficos
Autores principales: Moar, Agata, Bruni, Manfredo, Schena, Donatella, Rigotti, Erika, Colato, Chiara, Novelli, Antonio, Cesario, Claudia, Girolomoni, Giampiero
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8614091/
https://www.ncbi.nlm.nih.gov/pubmed/34853685
http://dx.doi.org/10.1002/ccr3.5108

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8614091/
https://www.ncbi.nlm.nih.gov/pubmed/34853685
http://dx.doi.org/10.1002/ccr3.5108

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