Naegeli-Franceschetti-Jadassohn syndrome: a systematic review of case studies

IntroductionNaegeli-Franceschetti-Jadassohn syndrome (NFJS), also known as Naegeli Syndrome, is a rare autosomal dominant ectodermal dysplasia characterized by mutations in the KRT14 gene. These mutations disrupt ectodermal tissue development, leading to diverse clinical manifestations involving the...

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Hlavní autoři:	Hussain Haider Shah, Tooba Hussain, Arun Subash, Ramsha Abdul Qadir, Yashika Rajesh Meshram, Maryam Shahzad, Wania Sultan, Zeenat Hadi, Faiza Ashfaque, Zahra Anas, Sameer Abdul Rauf, Radeyah Waseem, Muhammad Sheheryar Hussain, Muhammad Abdul Wasay Zuberi
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	Frontiers Media S.A. 2025-02-01
Edice:	Frontiers in Medicine
Témata:	Naegeli-Franceschetti-Jadassohn syndrome NFJS dermatological disorders clinical presentation systematic review
On-line přístup:	https://www.frontiersin.org/articles/10.3389/fmed.2025.1453172/full
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