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Naegeli–Franceschetti–Jadassohn syndrome: A rare case

Naegeli–Franceschetti–Jadassohn Syndrome (NFJS) is a rare, autosomal dominant inherited form of ectodermal dysplasia, caused by mutation in the KRT14 gene. We report here a case of NFJS in a 27-year-old male who presented with reticulate hyperpigmentation over skin, dental changes, absence of dermat...

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Detalles Bibliográficos
Autores principales:	Shah, Bela J., Jagati, Ashish K., Gupta, Neha P., Dhamale, Suyog S.
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/PMC4693352/ https://www.ncbi.nlm.nih.gov/pubmed/26753140 http://dx.doi.org/10.4103/2229-5178.169712

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