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Pediatric Dermatology, Volume 41, Issue 6, Page 1106-1113, November/December 2024.ABSTRACT Background Focal dermal hypoplasia (FDH), also known as Goltz syndrome, is a rare ectodermal dysplasia that primarily affects the skin, skeleton, and eyes. It is an X‐linked dominant disorder, predominantly seen in females, caused by pathogenic variants in PORCN. Methods We characterized a case series of four genetically confirmed FDH patients
Laura Krogh Herlin +6 more
wiley +1 more source
Gorlin-Goltz: what's in a name?
, 1998 This paper describes the clinical features of two very distinct syndromes with similar names: Gorlin-Goltz and Goltz-Gorlin Syndromes. A case report is presented that highlights the differences between these syndromes.
Trotman, C A, Russell, K A, McNamara, T
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, 2023 Analysis of basal cell carcinomas' histological subtypes and relative response to vismodegib in six patients diagnosed with Gorlin–Goltz syndrome: A retrospective ...
Melotti B. +6 more
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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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Examine your orofacial cleft patients for Gorlin-Goltz syndrome.
, 1997 The Gorlin-Goltz syndrome is characterized by four primary symptoms: multiple nevoid basal cell epitheliomas that usually undergo malignant transformation; jaw keratocysts that show constant growth; skeletal anomalies; and intracranial calcifications.
Kreusch T, Lambrecht JT
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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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