Results 51 to 60 of about 7,017,185 (188)

Diagnostic Accuracy of Artificial Intelligence Models for Detecting Odontogenic Keratocytes on CBCT Imaging: A Systematic Review and Meta‐Analysis

Health Science Reports, Volume 9, Issue 9, September 2026.
ABSTRACT Background and Aims Differentiating odontogenic keratocyst (OKC) from other radiolucent jaw lesions like ameloblastoma is clinically important but radiographically difficult. Recent advances in artificial intelligence (AI) show promise for enhancing diagnosis using cone‐beam computed tomography (CBCT).
Reyhaneh Shoorgashti, Simin Lesan, Sarah Sadat Ehsani, Asma Yazdanfar   +3 more
wiley   +1 more source

Basal Cell Carcinoma, Odontogenic Cysts, Brain and Skeletal Abnormalities (Gorlin Goltz) Syndrome in a 46-Year-Old Woman

Philippine Journal of Otolaryngology Head and Neck Surgery, 2018
Objective: To present the case of a 46-year-old woman with basal cell carcinoma, odontogenic cysts, brain anomalies and skeletal abnormalities. Method:             Design:           Case Report             Setting:           Tertiary National ...
Diane Clarice D. Magbuhat, Jeannette Marie S. Matsuo, Rhodieleen Anne R. de la Cruz   +2 more
doaj   +1 more source

Nonsyndromic cases of multiple odontogenic keratocyst: Series of two cases

MRIMS Journal of Health Sciences, 2022
Odontogenic keratocysts (OKCs) are developmental odontogenic cyst of epithelial origin. Multiple OKCs are often associated with a syndrome, especially nevoid basal cell carcinoma syndrome.
Aishwarya Bhopathi, Chunduri Nagendra Srinivas, Yousuf Qureshi Mohd, Anita Parushetti   +3 more
doaj   +1 more source

Elongated Styloid Process Associated With Nevoid Basal Cell Carcinoma Syndrome

, 2011
This article presents a case with nevoid basal cell carcinoma syndrome (NBCCS) and an elongated styloid process. Basal cell carcinoma syndrome, also known as Gorlin-Goltz syndrome, is an autosomal dominant inherited syndrome manifested by multiple ...
ATALAR, MEHMET HAYDAR, Durmus, Kasm, Atalar, Mehmet H., Kosar, Mehmet Ilkay, Mehmet H. Atalar, Mehmet İlkay Koşar, Uysal, Ismail Onder, İsmail Önder Uysal, Kasm Durmuş   +8 more
core   +1 more source

Gorlin-Goltz Syndrome

Case Reports in Dentistry, 2012
The Gorlin-Goltz syndrome (GGS) (the nevoid basal cell carcinoma syndrome—NBCCS) is a rare autosomal dominant syndrome caused due to mutations in the PTCH (patched) gene found on chromosome arm 9q.
Padma Pandeshwar, K. Jayanthi, D. Mahesh
doaj   +1 more source

The WHO Classification of Genetic Tumour Syndromes: Considerations for Genetics

Clinical Genetics, Volume 110, Issue 3, Page 389-401, September 2026.
The WHO Classification of Tumours underpins the diagnosis of neoplastic conditions. The new WHO classification of genetic tumour syndromes (GTS) provides international standards for their diagnosis. This diagram highlights the chromosomal distribution of the genes involved in the GTS covered in this classification.
Ian A. Cree, Mark J. Arends, Joseph D. Khoury, Erika R. E. Denton, Anthony J. Gill, Alexander J. Lazar, Ian M. Frayling, Stefan M. Pfister, Mark A. Rubin, Katia R. M. Leite, Raymond Dalgleish, Elspeth A. Bruford, Sharon E. Plon, Ada Hamosh, Michael Francis Walsh, Gabrielle Goldman‐Lévy, Harshima Wijesinghe, William D. Foulkes, Dilani Lokuhetty   +18 more
wiley   +1 more source

Nevoid basal cell carcinoma syndrome

Journal of Oral Diagnosis, 2016
The nevoid basal cell carcinoma syndrome (NBCCS) is an autosomal dominant disorder with complete penetrance and variable expressivity. It is caused by mutations in the patched gene, mapped to chromosome 9q22.3-q31. Its characteristics include multiple basal cell carcinomas, odontogenic keratocysts, vertebral and rib anomalies, and intracranial ...
Lucielma Salmito Soares Pinto, Román Carlos-Bregni, Hercílio Martelli Júnior, Mário Rodrigues Melo Filho, null Wilson Delgado Azañero, Jorge Esquiche León, Márcio Ajudarte Lopes, Oslei Paes Almeida, Jacks Jorge   +8 more
openaire   +1 more source

A novel germline mutation in a patient with nevoid basal cell carcinoma syndrome showing cystic lesion in the lung [PDF]

, 2015
Nevoid basal cell carcinoma syndrome (NBCCS) manifests multiple defects involving the skin, endocrine and nervous systems, eyes and bones. Mutations in the patched homologue 1 (PTCH1) gene are the underlying causes of NBCCS, leading to aberrant cell ...
田久保, 康隆, Kurosawa, Manabu, 伊達, 洋至, Matsuda, Fumihiko, Miyata, Ryo, 松田, 文彦, 宮田, 亮, Kono, Tomoya, Shinkura, Reiko, 黒澤, 学, 河野, 朋哉, Takubo, Yasutaka, Okai, Shinsaku, Sato, Masaaki, 佐藤, 雅昭, Yamada, Keisuke, Date, Hiroshi   +16 more
core   +2 more sources

Enhancing Communication and Consent Using 3‐D Printed Models With a Pediatric Dental Patient Presenting With Odontogenic Keratocysts Associated With Gorlin Syndrome: A Case Report

Special Care in Dentistry, Volume 46, Issue 5, September/October 2026.
ABSTRACT Aims This case report aimed to describe the use of a patient‐specific 3D printed model to support communication and informed consent in a pediatric patient diagnosed with Gorlin syndrome, a rare condition frequently associated with multiple odontogenic keratocysts.
Romain Jacq, Margaux Picherit, Anne‐Charlotte Bas   +2 more
wiley   +1 more source

Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome

, 1996
The nevoid basal cell carcinoma syndrome (NBCCS) is an autosomal dominant disorder characterized by multiple basal cell carcinomas (BCCs), pits of the palms and soles, jaw keratocysts, a variety of other tumors, and developmental abnormalities.
Dean, M, Toftgard, R, Smyth,, Vorechovsky,, Wicking, C, Bale, AE, Chidambaram, A, Shanley, S, Negus, K, Pressman, C, Wainwright, B, ChenevixTrench, G, Vorechovsky, I, Goldstein, AM, Hahn, H, Gailani, MR, Leffell, DJ, Holmberg, E, Gillies, S, Unden, AB, Zaphiropoulos, PG, Gerrard, B   +21 more
core   +1 more source