Results 31 to 40 of about 1,227,185 (144)

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

Worth the Effort: Lessons for Discovery and Care From an Unusual Case of Gorlin Syndrome. [PDF]

Am J Med Genet A
ABSTRACT Gorlin‐Goltz Syndrome (GGS) is a rare autosomal dominant genetic disorder encompassing a diverse range of clinical manifestations, including congenital anomalies and predisposition to cancer. Pathogenic variants in PTCH1 and SUFU account for up to 79% and 6% of cases, respectively. Currently, an estimated 15%–27% of individuals with a clinical
Taliercio V, Zhao J, Boyden SE, Mao R, Bayrak-Toydemir P, Pflaum A, Palumbos J, Andrews A, Baldwin EE, Welt C, Fait M, Undiagnosed Diseases Network, Botto LD, Viskochil D.   +13 more
europepmc   +2 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

Vulvar Apocrine Hidrocystoma: A Rare Case Report. [PDF]

Case Rep Obstet Gynecol
Apocrine hidrocystoma is a rare and benign tumor that usually occurs on the head, neck, and face. Involvement of the vulva is extremely rare, with only a few documented case reports in the literature. The prognosis of the tumor is favorable with surgical excision, with no reported recurrences.
Mahmoudnejad N, Torbati PM, Irandoost N.
europepmc   +2 more sources

Basal Cell Nevus Syndrome Treated With Laser Therapy: Novel Approach for Young Adults. [PDF]

Int J Dermatol
International Journal of Dermatology, Volume 65, Issue 2, Page 362-364, February 2026.
Briatico G, Scharf C, Di Brizzi EV, Brancaccio G, Drmac N.   +4 more
europepmc   +2 more sources

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

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