Results 11 to 20 of about 1,227,185 (144)

Gorlin-Goltz Syndrome

open access: yesJournal 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   +3 more
doaj   +2 more sources

Gorlin-Goltz syndrome

open access: yesDental 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   +2 more
doaj   +4 more sources

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

open access: yesJournal 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   +3 more
doaj   +2 more sources

Gorlin syndrome - an incidental radiographic detection [PDF]

open access: yesSouth 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   +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

open access: yesIndian 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   +4 more
doaj   +2 more sources

Gorlin-goltz syndrome

open access: yesJournal 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   +5 more
doaj   +2 more sources

Multiple jaw cysts-unveiling the Gorlin-Goltz syndrome

open access: yesContemporary 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   +3 more
doaj   +2 more sources

Gorlin Goltz syndrome: A clinicopathological case report

open access: yesJournal 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   +3 more
doaj   +2 more sources

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

open access: yesClinical 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   +6 more
doaj   +8 more sources

A Case Report of Gorlin-goltz Syndrome

open access: yesJournal 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   +2 more
doaj   +1 more source

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