Naegeli-Franceschetti-Jadassohn syndrome in a Saudi Arabian family

J Forensic Sci. 2014 Mar;59(2):555-8. doi: 10.1111/1556-4029.12316. Epub 2013 Nov 21.

Abstract

In the course of applying to become a soldier, a 23-year-old Saudi Arabian man was found to have no fingerprints. Further medical examination has been carried out for the young man and for the rest of family members including two sisters, mother, and brothers except the father who had died sometime previously. Subsequent medical investigations suggested that he and his two brothers displayed most of the features of the Naegeli-Franceschetti-Jadassohn (NFJ) syndrome. These features included skin changes with hypo- and hyperpigmentation, hypohidrosis, dystrophy of the nails, diffuse thickening of the palms and feet, a lack of fingerprints (dermatoglyphics), and atrophic changes in the skin of the face; there were also dental anomalies. A typical feature of the Naegeli-Franceschetti-Jadassohn syndrome was found in a Saudi Arabian family. The aim of this study was to present this rare condition affecting a Saudi Arabian family and review the current literature on the subject.

Keywords: Naegeli-Franceschetti-Jadassohn Syndrome; dermatoglyphics; dystrophy of the nails; fingerprints; forensic pathology; forensic science; hyperpigmentation; hypohidrosis.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Adult
  • Ectodermal Dysplasia / diagnosis*
  • Ectodermal Dysplasia / genetics*
  • Female
  • Humans
  • Hypohidrosis / diagnosis*
  • Hypohidrosis / genetics*
  • Keratoderma, Palmoplantar / diagnosis*
  • Keratoderma, Palmoplantar / genetics*
  • Male
  • Pigmentation Disorders / diagnosis
  • Pigmentation Disorders / genetics
  • Rare Diseases / diagnosis
  • Rare Diseases / genetics
  • Saudi Arabia
  • Young Adult

Supplementary concepts

  • Naegeli syndrome