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Last Updated: 10/31/2025
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Found 9 publications
Naegeli-Franceschetti-Jadassohn syndrome: a systematic review of case studies.
Journal: Frontiers in medicine
Published: June 22, 2024
Identification of a founder mutation in KRT14 associated with Naegeli-Franceschetti-Jadassohn syndrome.
Journal: The British journal of dermatology
Published: April 14, 2020
Naegeli-Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis: intrafamilial overlap of phenotypes in patients with the same KRT14 frameshift variant.
Journal: The British journal of dermatology
Published: April 11, 2019
Naegeli-Franceschetti-Jadassohn syndrome in a Saudi Arabian family.
Journal: Journal of forensic sciences
Published: September 02, 2012
A new case of keratin 14 functional knockout causes severe recessive EBS and questions the haploinsufficiency model of Naegeli-Franceschetti-Jadassohn syndrome.
Journal: The Journal of investigative dermatology
Published: July 08, 2011
Prenatal and postnatal growth retardation, microcephaly, developmental delay, and pigmentation abnormalities: Naegeli syndrome, dyskeratosis congenita, poikiloderma Clericuzio type, or separate entity?
Journal: European journal of medical genetics
Published: October 06, 2010
Spontaneous fading of reticular pigmentation in Naegeli-Franceschetti-Jadassohn syndrome.
Journal: Dermatology (Basel, Switzerland)
Published: July 01, 2010
Thrombasthenia--a rare cause of Sheehan's syndrome.
Journal: Acta obstetricia et gynecologica Scandinavica
Published: July 01, 1995
Incontinentia pigmenti, Franceschetti-Jadassohn's syndrome
Journal: Przeglad dermatologiczny
Published: May 01, 1956
Showing 1-9 of 9
Last Updated: 10/31/2025