Naegeli–Franceschetti–Jadassohn syndrome: A rare reticulate pigmentary disorder

Abstract

Naegeli–Franceschetti–Jadassohn syndrome is a rare autosomal dominant form of ectodermal dysplasia affecting sweat glands, nails, teeth, and skin. We report a case of 16-year-old female who had generalized reticulate pigmentation, dental changes, nail changes, and absence of dermatoglyphics and hypohydrosis.

Keywords

• Dermatoglyphics
• ectodermal dysplasia
• KRT 14 gene
• Naegeli–Franceschetti–Jadassohn syndrome
• reticulate pigmentation