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SYNDROME DE GORLIN-GOLTZ : DIAGNOSTIC, PRISE EN CHARGE THERAPEUTIQUE ET SUIVI
Le syndrome de Gorlin-Goltz ou Naevomatosebaso-cellulaire est une affection hereditaire rare, decrite initialement en 1984 par JARISCH mais cest Gorlin et Goltz qui, en 1960, la definissent.
Adam Benbachir +7 more
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Le syndrome de Gorlin-Goltz : rapport d’un cas
, 2014 Les auteurs présentent la prise en charge d’un patient atteint d’une polykystose maxillo- mandibulaire. Compte tenu des antécédents familiaux et du diagnostic histologique qui met en évidence des kératokystes multiples, on évoque chez
Monica Umana, Thierry Piral
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Jaw cyst-Basal cell nevus-Bifid rib syndrome: A case report
Journal of Indian Society of Pedodontics and Preventive Dentistry, 2007 Jaw cyst-Basal cell nevus-Bifid rib syndrome or Gorlin-Goltz syndrome involves multiple organ system. The most common findings include multiple odontogenic keratocysts in the jaws and basal cell nevus on the skin that have an early age onset.
Rai S, Gauba K
doaj
THE EXPERIENCE OF TREATMENT OF MULTIPLE BASALIOMA IN GORLIN-GOLTZ SYNDROME
Alʹmanah Kliničeskoj Mediciny, 2016 Aim: To assess clinical efficacy of the treatment options for multiple basalioma in patients with Gorlin-Goltz syndrome. Materials and methods: We retrospectively analyzed the results of various treatments in 23 patients with the Gorlin-Goltz syndrome ...
E. I. Tret'yakova
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The Gorlin-Goltz syndrome: case report.
, 1990 Focal dermal hypoplasia is a syndrome characterized by anomalies of cutaneous, osseous, dental and ocular structures. Because of the ocular anomalies, this syndrome should be regarded as a fifth type of phakomatosis.
MAGLI, Adriano +3 more
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Incidence of Odontogenic Keratocysts in Patients with Gorlin-Goltz Syndrome according to Age, Gender and Location [PDF]
, 2004 Svrha ovoga rada bila je prikazati nastanak odontogenih keratocista (OKC) i keratocistama sličnih lezija u oboljelih od Gorlin-Goltzova sindroma s obzirom na dob i spol bolesnika te na mjesto nastanka OKC-a (donja čeljust, gornja čeljust, meka tkiva i ...
Pavelić, Božidar +5 more
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Gorlin-Goltz syndrome: A rare case report
, 2013 Gorlin-Goltz syndrome is an uncommon autosomal dominant inherited disorder characterized by numerous basal cell carcinomas, odontogenic keratocysts (OKCs) and musculoskeletal malformations.
Ritesh R Kalaskar +3 more
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Gorlin-Goltz Syndrome: A Case Series. [PDF]
Cureus, 2023 Salahudheen A +4 more
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Gorlin-goltz syndrome, an incidental finding: A rare case report
Journal of Indian Academy of Oral Medicine and Radiology, 2012 Gorlin-Goltz syndrome is an uncommonly found rare disease which shows various possible diverse manifestations of multisystem anomalies, high degree penetration rate with variable expressiveness at least on three body systems.
Sanyasi Gandhiraj
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Anaesthetic management in Gorlin-Goltz syndrome
, 2012 Gorlin-Goltz syndrome is a rare autosomal-dominant syndrome related to mutation in " Patched" tumour suppressor gene on chromosome 9. Basocellular carcinomas, odontogenic keratocysts, palmar and/or plantar pits and ectopic calcifications of the falx ...
Kundan S Gosavi, Surbhi D Mundada
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