Results 81 to 90 of about 1,227,280 (190)

Gorlin Goltz Syndrome : A Review

, 2003
Gorlin syndrome is a rare autosomal dominant disorder characterized by multiple basal cell carcinomas, odontogenic keratocysts, tumors, and systemic anomalies.
Anita Balan, C Raphy Paul, M S Deepa
core  

Multiple abdominal cysts in a patient with Gorlin-Goltz syndrome: a case report

, 2013
A rare case of symptomatic mesenteric cysts in a patient with Gorlin-Goltz syndrome, associated with various neoplasms, is presented. The patient, known with Gorlin-Goltz syndrome, consulted with increasingly severe abdominal pain and large abdominal ...
Hubens, G, Haenen, F, Creytens, David, Vaneerdeweg, W, Haenen, F., Creytens, D., Hubens, G., Vaneerdeweg, W.   +7 more
core   +1 more source

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

Gorlin - goltz syndrome: a case report [PDF]

, 2012
Gorlin-Goltz syndrome, also known as basal cell nevus syndrome, is an uncommon, autosomal dominant inherited disorder, which is characterized by numerous basal cell carcinoma, odontogenic keratocysts and musculoskeletal malformations.
Muhammad, Layla, Haidar, Ahmad, Khaleel, Amera Kamal   +2 more
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An 8.9 year old girl with autism and Gorlin syndrome

, 2011
We present an 8.9 year old girl diagnosed with autism and macrocrania. Because of macrocrania, hypertelorism and epidermal punctiform lesions in the palm of the hand, Gorlin syndrome was clinically suspected and molecularly confirmed by finding a ...
Delbroek, Hanne, Legius, Eric, Eric Legius, Steyaert, Jean, Hanne Delbroek, Jean Steyaert   +5 more
core   +1 more source

Gorlin syndrome with osteoma in the maxillary sinus (case report) Gorlin sendromu: Radyolojik bulgular.

, 2004
Gorlin syndrome is a rare autosomal dominant disorder characterized by multiple basal cell carcinomas of the skin, odontogenic keratocysts of the jaw, various skeletal abnormalities, and lamellar falx calsifications.
ÖZTÜRK, MUSTAFA, Sevinç, Halil, Mavili, Ertugrul, ÖZYAZGAN, İRFAN   +3 more
core   +1 more source

Gorlin-Goltz Syndrome: Case Report of a Rare Hereditary Disorder

Case Reports in Dentistry, 2012
Introduction. Gorlin-Goltz syndrome is an inherited autosomal dominant disorder with complete penetrance and extreme variable expressivity. Case Report.
Ashutosh Agrawal, Aditi Murari, Sunil Vutukuri, Arun Singh   +3 more
doaj   +1 more source

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