Naegeli-Franceschetti-Jadassohn syndrome: A rare case
Bela J Shah1, Ashish K Jagati1, Neha P Gupta1
1Department of Dermatology, BJ Medical College, Civil Hospital, Ahmedabad, Gujarat, India.
Abstract:
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 dermatoglyphics, hypohidrosis, and hair changes.
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