Results 81 to 90 of about 1,573 (165)

Frameshift mutation in exon 17 of PTCH1 gene in Nevoid basal cell carcinoma syndrome: A case report. [PDF]

J Oral Maxillofac Pathol, 2023
Aravind T, Savithri V, Suresh R, Subash P.   +3 more
europepmc   +1 more source

Nevoid Basal Cell Carcinoma Syndrome.

Indian journal of dermatology, venereology and leprology, 2017
A 65 years old male developed nevoid basal cell carcinoma syndrome, manifesting as multiple basal cell epitheliomas, marked mutilation of the face and characteristic pitting on the palms and soles. Calcification of the falx cerebri and scoliosis of the lumbar spine were also seen.
F, Handa, Pradeep, Sharma, Sudarshan, Gupta   +2 more
openaire   +1 more source

Establishment of induced pluripotent stem cells derived from patients and healthy siblings of a nevoid basal cell carcinoma syndrome family. [PDF]

In Vitro Cell Dev Biol Anim, 2023
Nakase Y, Hamada A, Obayashi F, Kitamura N, Hata T, Yamamoto T, Okamoto T.   +6 more
europepmc   +1 more source

Management of multiple odontogenic keratocysts associated with nevoid basal cell carcinoma syndrome: a case report of 11-year follow-up. [PDF]

J Korean Assoc Oral Maxillofac Surg, 2022
Kim HM, Lim SJ, Cho YC, Sung IY, Son JH.
europepmc   +1 more source

Electrophysiological Study of Visual Pathways in Nevoid Basal Cell Carcinoma Syndrome Patients. [PDF]

Eye Brain, 2021
Moramarco A, Alisi L, Lambiase A, Giustini S, Lucchino L, Miraglia E, Roberti V, Nebbioso M.   +7 more
europepmc   +1 more source

Proposed criteria for nevoid basal cell carcinoma syndrome in children assessed using statistical optimization. [PDF]

Sci Rep, 2021
Gold NB, Campbell IM, Sheppard SE, Tan WH.   +3 more
europepmc   +1 more source

Nevoid basal cell carcinoma syndrome with anophthalmia: a case report. [PDF]

Hua Xi Kou Qiang Yi Xue Za Zhi, 2022
Chen M, Tao S, Chen G, Tang Y, Mai H.
europepmc   +1 more source

Medulloblastoma with Extensive Nodularity in a Child with Gorlin Syndrome - Case Report from Regional Cancer Centre

Clinical Pediatric Hematology-Oncology
Gorlin syndrome, also known as Gorlin-Goltz syndrome, nevoid basal cell carcinoma syndrome (NBCCS), or basal cell nevus syndrome, is a rare autosomal dominant cancer predisposition disorder characterized by high penetrance and variable expressivity.
M. Vijay Krishnan, Appaji Lingegowda, Arun Kumar, Prakruthi S. Kaushik, Meena Haldorai, R. Nikila, Avinash Thummalapalli, T. M. Surekha   +7 more
doaj   +1 more source

From the diagnosis of a mandibular cystic lesion to the surgical management of a case of a nevoid basal cell carcinoma syndrome

Journal of Oral Medicine and Oral Surgery
Introduction: Gorlin-Goltz syndrome or nevoid basal cell carcinoma syndrome is a rare hereditary disease with autosomal dominant transmission. Multiple basal cell carcinomas, keratocysts located in the jaw, and developmental abnormalities are common ...
Khenifi Houcem, Rohart Justine, Moizan Hervé, Benateau Hervé   +3 more
doaj   +1 more source

Clinical and genetic profiling of nevoid basal cell carcinoma syndrome in Korean patients by whole-exome sequencing. [PDF]

Sci Rep, 2021
Kim B, Kim MJ, Hur K, Jo SJ, Ko JM, Park SS, Seong MW, Mun JH.   +7 more
europepmc   +1 more source