Results 91 to 100 of about 1,226,922 (193)

A case report of Gorlin-Goltz syndrome as a rare hereditary disorder

Journal of Research in Medical Sciences, 2011
Gorlin-Goltz syndrome is an autosomal dominant and a rare hereditary disease. Diagnosis of this syndrome is based on major and minor criteria. We report a Gorlin-Goltz syndrome in a 25-year-old male who was presented with progressive pain of maxilla and ...
Mehri Sirous, Nazila Tayari
doaj  

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
core   +1 more source

A Rare Disease in Children: Goltz Syndrome [PDF]

, 2016
Goltz sendromu (Fokal dermal hipoplazi), mezoektodermal dokuyu tutan ve çok nadir görülen bir hastalıktır. Deri lezyonları ile birlikte iskelet sistemi, dental ve oküler anomaliler, hastaların az bir kısmında da kalp ve böbrek anomalileri ...
Aslan, Eyüp, Bilgiç, Özlem, Çimen, Derya, Güvenç, Osman, Arslan, Derya, Oran, Bülent   +5 more
core  

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 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, Manzi G, Liguori G., Pignalosa B   +3 more
core  

Lung disease recalling paraseptal emphysema in a patient with Goltz syndrome

, 2016
Background: Goltz syndrome is a rare, genetic disorder mainly occurring in female patients. Case presentation: The case presented here is, to the best of our knowledge, the first description of the occurrence of lung parenchymal alterations in a young ...
Boggini T., Savasta S., Trabatti C., Savasta S, Cortese R., Dore R, Boggini T, Trabatti C, Di Stasi S., Stella G. M., Cortese R, Di Stasi S, Dore R., Stella GM   +13 more
core   +1 more source

Nevoid basal cell carcinoma syndrome (Gorlin syndrome): a case report

Journal of Medical Case Reports
Background Basal cell nevus syndrome, also known as Gorlin or Gorlin–Goltz syndrome, is a hereditary condition caused by mutation in the PATCHED gene.
Noura Abdul Rahman, Fatima Breim, Joud Zakour, Zainab Srouji, Silva Ishkhanian   +4 more
doaj   +1 more source

Gorlin-Goltz Syndrome: A Case Series. [PDF]

Cureus, 2023
Salahudheen A, Haidry N, Mokhtar EA, Shivhare P, Gupta V.   +4 more
europepmc   +1 more source

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, Chetan A Pol, Suvarna K Ghige, Suchitra R Gosavi   +3 more
core   +1 more source

Gorlin-Goltz Syndrome: Report of a Rare Case with an Update on the Review of the Literature. [PDF]

Contemp Clin Dent, 2023
Attur S, Patel JK, Attur K, Menat S.
europepmc   +1 more source