Results 11 to 20 of about 1,227,204 (153)

Identification of a PORCN c.1093C>T (p.Arg365Trp) Variant in a 12‐Year‐Old Girl With Goltz–Gorlin Syndrome

Clinical Case Reports
We report the first female case of Goltz–Gorlin syndrome with the PORCN c.1093C>T (p.Arg365Trp) variant, previously described only in a male with Klinefelter syndrome. This case expands the known phenotypic and genotypic spectrum of FDH.
Anna Bolzon, Francesca Caroppo, Lisa Passaglia, Francesca Boaretto, Leonardo Salviati, Anna Belloni Fortina   +5 more
doaj   +3 more sources

Gorlin-Goltz Syndrome

Journal of Indian Academy of Oral Medicine and Radiology, 2010
Gorlin-Goltz syndrome, also known as basal cell nevus syndrome, is an uncommon autosomal dominant inherited disorder characterized by numerous basal cell carcinomas, odontogenic keratocysts, and musculoskeletal malformation. It is occasionally associated
M K Sunil, Raghav Kumar, E N Guru, Vikash Ranjan   +3 more
doaj   +2 more sources

Gorlin-Goltz syndrome

Dental Research Journal, 2012
Gorlin-Goltz syndrome is an uncommon autosomal dominant inherited disorder, which is characterized by multiple odontogenic Keratocysts and basal cell carcinomas, skeletal, dental, ophthalmic, and neurological abnormalities, intracranial ectopic ...
Priya Shirish Joshi, Vijay Deshmukh, Someshwar Golgire   +2 more
doaj   +4 more sources

Gorlin-Goltz Syndrome with Multiple OKC in a 10-Year-Old Child: A Case Report [PDF]

Journal of Multidisciplinary Dental Research
Gorlin-Goltz syndrome is rare multi-system disease, which is, characterized by neoplasms and other developmental abnormalities. 1 It is a hereditary condition inherited as an autosomal dominant trait and caused by abnormalities in the PTCH1 ...
Devadhakshayani Venkatesan, Nandhini B Selvarajan, Yash Suraj Latkar, D Vinola   +3 more
doaj   +2 more sources

Gorlin syndrome - an incidental radiographic detection [PDF]

South African Journal of Radiology, 2011
Gorlin-Goltz syndrome (also known as nevoid basal cell carcinoma syndrome) was first reported in 1894, but described by Gorlin and Goltz in 1960 as a distinct entity consisting of ectodermal and mesodermal abnormalities.
Shishir Ram Shetty, K M Veena, Laxmikanth Chatra, Prashanth Shenai, Prasanna Kumar Rao, Jagadish Chandra   +5 more
doaj   +2 more sources

Oral diffuse B-cell non-Hodgkin′s lymphoma associated to Gorlin-Goltz syndrome: A case report with one year follow-up

Indian Journal of Pathology and Microbiology, 2011
Nevoid cell carcinoma syndrome or Gorlin-Goltz syndrome is an autosomal dominant disorder characterized by multiple basal cell carcinoma, multiple keratocyst tumors, and skeletal anomalies.
Cláudio M Pereira, Ana Paula M Lopes, Alexandre J Meneghini, Alberto F Silva, Tessa de L. Botelho   +4 more
doaj   +2 more sources

Gorlin-goltz syndrome

Journal of Indian Academy of Oral Medicine and Radiology, 2011
Gorlin-Goltz syndrome also known as nevoid basal cell carcinoma syndrome (NBCCS) is an infrequent multisystemic disease inherited in a dominant autosomal way, which shows a high level of penetrance and variable expressiveness.
B V Shobha, S Mosby, N Barkha, Biswajeet, M Ajit, T Deepak   +5 more
doaj   +2 more sources

Multiple jaw cysts-unveiling the Gorlin-Goltz syndrome

Contemporary Clinical Dentistry, 2015
Gorlin-Goltz syndrome or basal cell nevus syndrome is a comparatively rare syndrome characterized by basal cell nevi, odontogenic keratocysts, and skeletal anomalies. Diagnosis is based on the major and minor clinical and radiographic criteria.
S Manjima, Zameera Naik, Vaishali Keluskar, Anjana Bagewadi   +3 more
doaj   +2 more sources

Gorlin Goltz syndrome: A clinicopathological case report

Journal of Indian Academy of Oral Medicine and Radiology, 2014
The Gorlin-Goltz syndrome is an infrequent multisystemic disease, which is inherited in an autosomal dominant manner. This shows a high level of penetrance and variable expressiveness, characterized by multiple basal cell nevi or carcinomas, odontogenic ...
Shobha C Bijjaragi, Ashwinirani Suragimath, Varsha Ajit Sangle, Veerendra S Patil   +3 more
doaj   +2 more sources

Gorlin-Goltz Syndrome: case report and review of literature [PDF]

Clinical and Biomedical Research, 2014
Description of a case report of Gorlin-Goltz Syndrome diagnosed in a male newborn who presented increased head circumference and bifid ribs. Mother and grandmother presented typical physical findings of the syndrome, including palmar pits, odontogenic ...
Adrianne Rahde Bischoff, Yina Mercedes Timana Delgado, Fabiano de Oliveira Poswar, Eduardo Tarasconi Ruschel, Eduardo Kohls Toralles, Gabriel Lona Curubeto Lona de Miranda, Mario Francisco Silveira Rita   +6 more
doaj   +6 more sources