Results 61 to 70 of about 5,083 (170)

Síndrome de Gorlin-Goltz: revisão das características neurorradiológicas e maxilofaciais ilustradas com dois casos.

Acta Médica Portuguesa, 2010
Gorlin-Goltz syndrome or nevoid basal cell carcinoma syndrome is a rare hereditary autosomal-dominant disorder characterized by multiple basal cell carcinomas in young patients, odontogenic keratocysts, palmar or plantar pits, calcification of the falx ...
Marta Maia Safronova, Mavilde Arantes, Iva Lima, Sara Domingues, Marta Almeida, Pedro Moniz   +5 more
doaj   +1 more source

Naevoid Basal Cell Carcinoma Syndrome

مجله دانشکده پزشکی اصفهان, 2012
Nevoid basal cell carcinoma syndrome (NBCCS), also known as Gorlin syndrome, is a hereditary condition characterized by a wide range of developmental abnormalities and a predisposition to neoplasms.
Zabihollah Shahmoradi, Fateme Andalib, Amir Hossein Siadat   +2 more
doaj  

Gorlin's Syndrome [PDF]

Journal of the Royal Society of Medicine, 1985
MacSweeney, J E, Forbes, A, Manhire, A R, Lees, W R   +3 more
openaire   +3 more sources

Gorlin syndrome: A case report

Journal of Indian Society of Pedodontics and Preventive Dentistry, 2005
Gorlin syndrome is an autosomal dominant inherited condition that exhibits high penetrance and variable expressivity. It is characterized mainly by Basal cell carcinomas, Odontogenic keratocysts and skeletal anomalies.
Patil K, Mahima V, Gupta B
doaj  

Youngest Encounter with Gorlin–Goltz Syndrome: Navigating Early Diagnosis and Management

Indian Journal of Paediatric Dermatology
Gorlin–Goltz syndrome is a rare autosomal dominant disorder caused by an inactivating mutation of the patched 1 gene. Patients could present as early as infancy with varied presentation and multiple basal cell carcinoma.
Adarsh Vijayakumar, Rashmi Mary Philip, Sebastian Criton   +2 more
doaj   +1 more source

A Rare Case of Gorlin-Goltz Syndrome in Children

Case Reports in Dentistry, 2019
The Gorlin-Goltz syndrome, nevoid basal cell carcinoma syndrome, or basal cell nevus syndrome is an autosomal dominant condition disorder with high variability expression.
Fernanda Brasil Daura Jorge Boos Lima, Ana Paula Cota Viana, Luciano Henrique Ferreira Lima, Bruna Campos Ribeiro, Carlos Eduardo Assis Dutra, Glaykon Alex Vitti Stabile, Sergio Monteiro Lima Junior   +6 more
doaj   +1 more source

Focal dermal hypoplasia: A novel finding in disguise

Journal of Oral Biology and Craniofacial Research, 2018
Focal Dermal Hypoplasia (FDH) or Goltz-Gorlin syndrome is an unusual X-linked dominant syndrome characterised by anomalies of both ectodermal and mesodermal structures.We present a case report on the management of a 58 year old Caucasian male with Focal ...
S. Nathwani, K. Martin, R. Bunyan
doaj   +1 more source

Basal Cell Nevus Syndrome Treated With Laser Therapy: Novel Approach for Young Adults

International Journal of Dermatology, Volume 65, Issue 2, Page 362-364, February 2026.
Giulia Briatico, Camila Scharf, Eugenia Veronica Di Brizzi, Gabriella Brancaccio, Nikola Drmac   +4 more
wiley   +1 more source

SINDROME DE GORLIN: A PROPOSITO DE UN CASO Gorlin’s Syndrome: A case

Revista Habanera de Ciencias Médicas, 2008
El llamado Síndrome de Gorlin es un raroy poco frecuente desorden clínico-patológico hereditario de carácter autosómico dominante bien reconocido y expresión variable. El Síndrome se caracteriza por múltiples nódulos cutáneos en piel no expuesta al sol y
Concepción Pereira Dávalos, Joaquín Urbizo Vélez, Ana Dolores Mori Estévez   +2 more
doaj  

A Case Report of Gorlin-goltz Syndrome

Journal of Contemporary Medical Sciences, 2016
Nevoid basal cell carcinoma syndrome (Gorlin syndrome) is an autosomal dominant inherited condition that exhibits high penetrance and variable expressivity.
Shima Nafarzadeh, Fatemeh Mozaffari, Oveis Khakbaz   +2 more
doaj