Results 81 to 90 of about 1,226,922 (193)

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
core  

Novel Mutation in a Child with Goltz Syndrome

, 2011
Goltz syndrome or focal dermal hypoplasia is a rare clinical syndrome presenting with cutaneous, skeletal, dental, ocular, central nervous system and soft-tissue defects. The authors report a female child clinically diagnosed as Goltz syndrome, confirmed
Seema Kapoor, Kapoor, Seema, McGrath, John A., Atul Mohan Kochar, Kapoor, Harit, Reetika Malik, John A. McGrath, Kochar, Atul Mohan, Malik, Reetika, Harit Kapoor, Ghosh, Vidyabrata, Vidyabrata Ghosh   +11 more
core   +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

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

Argon laser surgery of mucous membranes papillomatosis in EEC syndrome and Goltz syndrome [PDF]

, 1991
This article describes successful results after argon laser surgery of verrucous and papillomatous lesions on the mucous membranes of the lips in two patients; the first with the EEC syndrome and the second with the Goltz syndrome.
Hernandez, D. A., Pasyk, Krystyna A.
core   +1 more source

Gorlin-Goltz: what's in a name?

, 1998
This paper describes the clinical features of two very distinct syndromes with similar names: Gorlin-Goltz and Goltz-Gorlin Syndromes. A case report is presented that highlights the differences between these syndromes.
Trotman, C A, Russell, K A, McNamara, T
core  

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

Expanding the Interface: Overlooked Dermatologic Disorders With Ocular Involvement

JEADV Clinical Practice, Volume 4, Issue 5, Page 1239-1243, December 2025.
A George
wiley   +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

Goltz syndrome: A newborn with ectrodactyly and skin lesions

Indian Journal of Dermatology, 2015
Goltz syndrome or Focal Dermal Hypoplasia is a rare multisystem disorder, involving all the three germ cell layers. The disease is thought to be inherited in X-linked dominant fashion with heterogeneous mutations of the PORCN gene at Xp11.23 locus ...
Shatanik Sarkar, Chaitali Patra, Amit Das, Sutirtha Roy   +3 more
doaj   +1 more source