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CASE REPORT
Year : 2015  |  Volume : 6  |  Issue : 6  |  Page : 403-406

Naegeli-Franceschetti-Jadassohn syndrome: A rare case


Department of Dermatology, BJ Medical College, Civil Hospital, Ahmedabad, Gujarat, India

Correspondence Address:
Bela J Shah
Department of Skin and VD, Room No. 139, 1st Floor, Wing No. 3, OPD Building, Civil Hospital, Asarwa, Ahmedabad, Gujarat
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/2229-5178.169712

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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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