Results 31 to 40 of about 1,227,254 (171)

Case Report: Sequential Treatment Strategy for Advanced Basal Cell Carcinoma in Gorlin-Goltz Syndrome: Integration of Vismodegib, Radiotherapy, Surgery, and High-Intensity Focused Ultrasound [PDF]

Frontiers in Oncology
Natalia Sauer, Ahmed Elsaftawy
exaly   +2 more sources

Syndrome in question: Gorlin-Goltz syndrome [PDF]

Anais Brasileiros de Dermatologia, 2016
The Nevoid Basal Cell Carcinoma Syndrome (NBCCS) is an uncommon disorder caused by a mutation in Patched, tumor suppressor gene. It is mainly characterized by numerous early onset basal cell carcinomas, odontogenic cysts of jaw and skeletal abnormalities. Due to the wide clinical spectrum, treatment and management of its modalities are not standardized
Pauline Lyrio Ribeiro, João Basílio de Souza Filho, Karina Demoner de Abreu, Marisa Simon Brezinscki, Christine Chambo Pignaton   +4 more
openaire   +3 more sources

Oral and Maxillofacial Perspective of Gorlin-Goltz syndrome: A Clinical Case Series of three Patients

King Khalid University Journal of Health Sciences, 2016
Gorlin-Goltz syndrome is an autosomal dominant inherited syndrome. It is also known as hereditary cutaneo-mandibular polyonocosis, multiple nevoid basal cell epithelioma-jaw cysts or bifid rib syndrome.
Nasser Alasseri, Heba Alqarni, Ahmed Alqarni, Farheen Ustad   +3 more
doaj   +1 more source

Gorlin-Goltz Syndrome

Indian Journal of Oral Health and Research, 2015
Gorlin-Goltz syndrome is an autosomal dominant disorder showing multiple organ involvement. The syndrome consists principally of nevoid basal cell carcinomas, keratocystic odontogenic tumors (KCOT), skeletal anomalies and intracranial calcifications. A case report of a 25-year-old female patient emphasizing its clinical and radiographic manifestations ...
Vasavi Krishnamurthy, Sunanda Bhatnagar, SS Pagare   +2 more
  +9 more sources

Basaloid follicular hamartoma associated with follicular mucinosis and inflammation

Anais Brasileiros de Dermatologia, 2022
Basaloid follicular hamartoma is a benign, superficial malformation of hair follicles that can be mistaken both clinical and histopathologically for basal cell carcinoma.
Solange Edelman, Adriana Natalia Torres Huamani, María Del Valle Centeno, Andrea Bettina Cervini   +3 more
doaj   +1 more source

Electrochemotherapy: a Valid Treatment for Gorlin Goltz syndrome [PDF]

, 2013
Gorlin-Goltz syndrome is a rare disorder, characterized by systemic manifestations included multiple basal cell carcinomas, palmar or plantar pits, odontogenic keratocysts and ectopic calcifications of the falx cerebri.
Calvieri, Stefano, Miraglia, Emanuele, Giustini, Sandra, Curatolo, Pietro, Rotunno, Roberta   +4 more
core   +1 more source

Tonsillar Hypertrophy in Goltz-Gorlin Syndrome: Case Report and Literature Review

B-ENT, 2023
Goltz-Gorlin syndrome, also known as focal dermal hypoplasia or nevoid basal cell carcinoma syndrome, is a rare multisystemic disease caused by autosomal dominant mutations in the PORCN gene.
Emilie Lavrysen, Bart Loeys, Olivier M. Vanderveken, An Boudewyns   +3 more
doaj   +2 more sources

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

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