Naegeli-Franceschetti-Jadassohn syndrome: A rare case

• Egile Nagusiak: Bela J Shah (Egilea), Ashish K Jagati (Egilea), Neha P Gupta (Egilea), Suyog S Dhamale (Egilea)
• Formatua: Liburua
• Argitaratua: Wolters Kluwer Medknow Publications, 2015-01-01T00:00:00Z.
• Gaiak: article
• Sarrera elektronikoa: Connect to this object online.

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...