Naegeli-Franceschetti-Jadassohn syndrome: A rare case

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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Bibliographic Details
Main Authors: Bela J Shah, Ashish K Jagati, Neha P Gupta, Suyog S Dhamale
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2015-01-01
Series:Indian Dermatology Online Journal
Subjects:
Dermatopathia pigmentosa reticularis
KRT 14 gene
Naegeli-Franceschetti-Jadassohn
reticulate hyperpigmentation
Online Access:http://www.idoj.in/article.asp?issn=2229-5178;year=2015;volume=6;issue=6;spage=403;epage=406;aulast=Shah

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http://www.idoj.in/article.asp?issn=2229-5178;year=2015;volume=6;issue=6;spage=403;epage=406;aulast=Shah

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