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  • Title: Naegeli-Franceschetti-Jadassohn syndrome: A rare case.
    Author: Shah BJ, Jagati AK, Gupta NP, Dhamale SS.
    Journal: Indian Dermatol Online J; 2015; 6(6):403-6. PubMed ID: 26753140.
    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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