Franceschetti-Jadassohn syndrome

Franceschetti-Jadassohn syndrome
a rare autosomal dominant disorder characterized by gray to brown reticular hyperpigmentation beginning after infancy without preceding inflammatory changes; characteristics include palmoplantar keratoderma, vasomotor changes with hypohidrosis, and yellowing of the dental enamel.

Medical dictionary. 2011.

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  • Franceschetti-Jadassohn syndrome — Fran·ce·schet·ti Jad·as·sohn syndrome (frahn″chĕ sketґe yahґdah sōn) [A. Franceschetti; Josef Jadassohn, German dermatologist, 1863–1936] see under syndrome …   Medical dictionary

  • Naegeli–Franceschetti–Jadassohn syndrome — Classification and external resources OMIM 161000 DiseasesDB 29767 eMedicine …   Wikipedia

  • Naegeli-Franceschetti-Jadassohn-Syndrom — Das Naegeli Syndrom, auch als Naegeli Franceschetti Jadassohn Syndrom (NFJS) beziehungsweise NFJ Syndrom bezeichnet, ist eine sehr seltene Erbkrankheit, die autosomal dominant vererbt wird. Es handelt sich um eine Form einer anhidrotischen… …   Deutsch Wikipedia

  • syndrome — The aggregate of symptoms and signs associated with any morbid process, and constituting together the picture of the disease. SEE ALSO: disease. [G. s., a running together, tumultuous concourse; (in med.) a concurrence of symptoms, fr. syn,… …   Medical dictionary

  • Franceschetti — Adolphe, Swiss ophthalmologist, 1896–1968. See F. syndrome, F. Jadassohn syndrome …   Medical dictionary

  • Jadassohn — Josef, German dermatologist in Switzerland, 1863–1936; introduced the patch test for contact dermatitis. See J. nevus, Borst J. type intraepidermal epithelioma, J. Pellizzari anetoderma, Franceschetti J. syndrome, J. Lewandowski syndrome …   Medical dictionary

  • Naegeli syndrome — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 29767 ICD10 = ICD9 = ICDO = OMIM = 161000 MedlinePlus = eMedicineSubj = derm eMedicineTopic = 736 MeshID = Naegeli syndrome (or Naegeli Franceschetti Jadassohn syndrome) [OMIM|161000] is a… …   Wikipedia

  • Marfan syndrome — Marfan redirects here. For the person after whom the syndrome is named, see Antoine Marfan. Marfan syndrome Classification and external resources Micrograph demonstrating myxomatous degeneration of the aorti …   Wikipedia

  • Tietz syndrome — Not to be confused with Tietze syndrome. Tietz syndrome Classification and external resources ICD 10 E70.3 (ILDS E70.358) OMIM 103500 …   Wikipedia

  • Usher syndrome — Classification and external resources OMIM 276900 276901 DiseasesDB 13611 …   Wikipedia

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