Results 101 to 110 of about 1,226,922 (193)
Gorlin-Goltz Syndrome - A Concatenation of Six Case Reports. [PDF]
Ann Maxillofac Surg, 2023 Marimallappa TR +5 more
europepmc +1 more source
A male with polysyndactyly, linear skin defects and sclerocornea. Goltz syndrome versus MIDAS
, 2002 Focal dermal hypoplasia (FDH) or Goltz syndrome is a rare clinical syndrome presenting with cutaneous, skeletal, dental, ocular, central nervous system and soft-tissue defects.
Fryssira, H +5 more
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Siblings with Gorlin-Goltz syndrome associated with cardiac tumors: a case report and review of literature. [PDF]
Orphanet J Rare Dis, 2023 Wilke PI +7 more
europepmc +1 more source
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
doaj
Headache as the presenting manifestation of Gorlin-Goltz syndrome with diastematomyelia: A case report. [PDF]
Neurol Clin Neurosci, 2023 Ghosh R +5 more
europepmc +1 more source
A Case Report of Gorlin-goltz Syndrome
, 2016 Nevoid basal cell carcinoma syndrome (Gorlin syndrome) is an autosomal dominant inherited condition that exhibits high penetrance and variable expressivity.
Shima Nafarzadeh +2 more
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Ankara Universitesi Dis Hekimligi Fakultesi dergisi = The Journal of the Dental Faculty of Ankara University, 1991 Gorlin-Goltz syndrome has mainly three components; basal cell carcinoma, jaw cysts and skeletal anomalies. However, various cases of this syndrome with over 40 different kinds of components have been reported. In this paper, a case with Gorlin-Goltz syndrome treated in our clinic have been presented and discussed.
K, Sevin, N, Kutlu, M O, Yenidünya
openaire +1 more source
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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Gorlin Goltz Syndrome: Beware of Melanoma. [PDF]
Dermatol Pract Concept, 2022 Russo F +5 more
europepmc +1 more source
Focal Dermal Hypoplasia (Goltz Syndrome): A Rare Case. [PDF]
Indian Dermatol Online J, 2022 Gupta I, Dhankar N, Dayal S, Tyagi M.
europepmc +1 more source