Results 31 to 40 of about 1,227,204 (153)

Oral manifestation of Goltz-Gorlin syndrome in a young girl [PDF]

, 2012
Introduction Focal dermal hypoplasia (Goltz-Gorlin syndrome) is a multi-system disorder characterized by involvement of skin, skeletal system, eyes and face. It is caused by loss-of-function mutations in the PORCN gene.
Clarich, G, G Clarich, Callea, M., Deroma, L, I Yavuz, Yavuz, I, Callea M, Montanari, Marco, Montanari, M, E Albertini, Garavelli L, Clarich G, Maglione M, Albertini, Enrico, Yavuz I, MAGLIONE, MICHELE, Deroma, Laura, Callea, M, Deroma L, L., Yavuz, İzzet, Garavelli, E. Albertini, L Garavelli, L Deroma, M Montanari, M Maglione, M Callea, Albertini E, Montanari M, Clarich, Gabriella   +29 more
core   +1 more source

Synchronous jawbone diseases: a multicenter retrospective study [PDF]

Brazilian Oral Research, 2023
The aim of this study is to report an original case series of synchronous jawbone diseases. Data of patients seen over 13 years were extracted from the files of three Oral Radiology and Pathology diagnostic centers in Brazil.
Diogo dos Santos da Mata REZENDE, Lucas Lacerda de SOUZA, Daniel Cavalléro Colares UCHÔA, Lais Albuquerque FERNANDES, Jeanne Gisele Rodrigues de LEMOS, Alan Roger SANTOS-SILVA, Márcio Ajudarte LOPES, Lady Paola Aristizabal ARBOLEDA, André Caroli ROCHA, Fábio Luiz Neves GONÇALVES, Flávia Sirotheau Corrêa PONTES, Felipe Paiva FONSECA, Hélder Antônio Rebelo PONTES   +12 more
doaj   +1 more source

Gorlin-Goltz syndrome: A rare case

Indian Journal of Dermatology, 2015
Gorlin-Goltz syndrome or nevoid basal cell carcinoma syndrome is characterized by multiple basocellular epitheliomas, keratocysts in the jaws, bifid ribs, palmar and/or plantar pits and ectopic calcifications of the falx cerebri.
Satyaki Ganguly, Kranti C Jaykar, Rajesh Kumar, Abhijeet Kumar Jha, P K Banerjee   +4 more
doaj   +1 more source

Unilateral Tonsillar Hypertrophy in a 4-Year-Old Girl with Focal Dermal Hypoplasia (Goltz Syndrome)

Philippine Journal of Otolaryngology Head and Neck Surgery, 2018
Objective: To report a case of unilateral tonsillar hypertrophy resulting in severe Obstructive Sleep Apnea in a 4-year-old girl with focal dermal hypoplasia (FDH, Goltz or Goltz-Gorlin) Syndrome. Methods: Design:           Case Report Setting:  
John Emmanuel L. Ong, Emmanuel Tadeus S. Cruz, Clydine Maria Antonette G. Barrientos   +2 more
doaj   +1 more source

Image_4_Congenital medulloblastoma in two brothers with SUFU-mutated Gorlin-Goltz syndrome: Case reports and literature review.tif

, 2022
BackgroundCongenital medulloblastoma is very rare, and many cases involve germline mutations that can lead to inherited syndromes. Here, we first report two brothers with congenital medulloblastoma who were diagnosed with Gorlin-Goltz syndrome caused by ...
Yang Zhao (39052), Jie Ma (166937), Haibo Zhang (5720), Yufan Chen (679519)   +3 more
core   +1 more source

Keratocystic odontogenic tumors related to Gorlin–Goltz syndrome: A clinicopathological study

Journal of Oral Biology and Craniofacial Research, 2016
Background: Assess clinicopathological features of patients with keratocystic odontogenic tumor (KCOT) associated with Gorlin–Goltz syndrome in our institution from 2004 to 2015.
Mohammed Israr Ul Khaliq, Ajaz A. Shah, Irshad Ahmad, Shahid Hasan, Sagar S. Jangam, Farah, Anwar   +6 more
doaj   +1 more source

Image_5_Congenital medulloblastoma in two brothers with SUFU-mutated Gorlin-Goltz syndrome: Case reports and literature review.tif

, 2022
BackgroundCongenital medulloblastoma is very rare, and many cases involve germline mutations that can lead to inherited syndromes. Here, we first report two brothers with congenital medulloblastoma who were diagnosed with Gorlin-Goltz syndrome caused by ...
Yang Zhao (39052), Jie Ma (166937), Haibo Zhang (5720), Yufan Chen (679519)   +3 more
core   +1 more source

Image_1_Congenital medulloblastoma in two brothers with SUFU-mutated Gorlin-Goltz syndrome: Case reports and literature review.tif

, 2022
BackgroundCongenital medulloblastoma is very rare, and many cases involve germline mutations that can lead to inherited syndromes. Here, we first report two brothers with congenital medulloblastoma who were diagnosed with Gorlin-Goltz syndrome caused by ...
Yang Zhao (39052), Jie Ma (166937), Haibo Zhang (5720), Yufan Chen (679519)   +3 more
core   +1 more source

From the diagnosis of a mandibular cystic lesion to the surgical management of a case of a nevoid basal cell carcinoma syndrome

Journal of Oral Medicine and Oral Surgery
Introduction: Gorlin-Goltz syndrome or nevoid basal cell carcinoma syndrome is a rare hereditary disease with autosomal dominant transmission. Multiple basal cell carcinomas, keratocysts located in the jaw, and developmental abnormalities are common ...
Khenifi Houcem, Rohart Justine, Moizan Hervé, Benateau Hervé   +3 more
doaj   +1 more source

Image_3_Congenital medulloblastoma in two brothers with SUFU-mutated Gorlin-Goltz syndrome: Case reports and literature review.tif

, 2022
BackgroundCongenital medulloblastoma is very rare, and many cases involve germline mutations that can lead to inherited syndromes. Here, we first report two brothers with congenital medulloblastoma who were diagnosed with Gorlin-Goltz syndrome caused by ...
Yang Zhao (39052), Jie Ma (166937), Haibo Zhang (5720), Yufan Chen (679519)   +3 more
core   +1 more source