Naegeli syndrome

Reticular skin changes, dental anomalies, decreased function of sweat glands, strabismus, and optic atrophy

Also Known As:

Naegeli-Franceschetti-Jadassohn Syndrome

Networked: 3 relevant articles (0 outcomes, 0 trials/studies)

1.	Dyskeratosis Congenita (X-Linked Dyskeratosis Congenita)
2.	Dowling-Degos Disease
3.	Dyschromatosis universalis hereditaria
4.	Dyschromatosis symmetrica hereditaria 1
5.	Dermatopathia pigmentosa reticularis

1.	Décha, Audrey: 1 article (10/2011)
2.	Gasc, Géraldine: 1 article (10/2011)
3.	Hovnanian, Alain: 1 article (10/2011)
4.	Mejía, José Enrique: 1 article (10/2011)
5.	Pironon, Nathalie: 1 article (10/2011)
6.	Prost-Squarcioni, Catherine: 1 article (10/2011)
7.	Titeux, Matthias: 1 article (10/2011)
8.	Tonasso, Laure: 1 article (10/2011)
9.	Bercovich, Dani: 1 article (06/2008)
10.	Bergman, Reuven: 1 article (06/2008)

Drugs and Important Biological Agents (IBA) related to Naegeli syndrome:

1.	Keratin-14 (Keratin 14)IBA 10/01/2011 - "A new case of keratin 14 functional knockout causes severe recessive EBS and questions the haploinsufficiency model of Naegeli-Franceschetti-Jadassohn syndrome."
2.	Tumor Necrosis Factor-alpha (Tumor Necrosis Factor)IBA 06/01/2008 - "KRT14 haploinsufficiency results in increased susceptibility of keratinocytes to TNF-alpha-induced apoptosis and causes Naegeli-Franceschetti-Jadassohn syndrome."
3.	Dichlorodiphenyldichloroethane (DDD)IBA 01/01/2023 - "Inherited RPDs include dyschromatosis symmetrica hereditaria (DSH), dyschromatosis universalis hereditaria (DUH), reticulate acropigmentation of Kitamura (RAK), Dowling-Degos disease (DDD), dyskeratosis congenita (DKC), Naegeli-Franceschetti-Jadassohn syndrome (NFJS), dermatopathia pigmentosa reticularis (DPR), and X-linked reticulate pigmentary disorder. "