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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Xehetasun bibliografikoak
Egile Nagusiak: Bela J Shah, Ashish K Jagati, Neha P Gupta, Suyog S Dhamale
Formatua: Artikulua
Hizkuntza:English
Argitaratua: Wolters Kluwer Medknow Publications 2015-01-01
Saila:Indian Dermatology Online Journal
Gaiak:
Dermatopathia pigmentosa reticularis
KRT 14 gene
Naegeli-Franceschetti-Jadassohn
reticulate hyperpigmentation
Sarrera elektronikoa:http://www.idoj.in/article.asp?issn=2229-5178;year=2015;volume=6;issue=6;spage=403;epage=406;aulast=Shah

Internet

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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