Filtered By:
Procedure: Radiography

This page shows you your search results in order of relevance.

Order by Relevance | Date

Total 34580 results found since Jan 2013.

An uncommon disorder with multiple skeletal anomalies: Gorlin-Goltz syndrome.
Abstract Gorlin-Goltz syndrome is an uncommon disorder transmitted through autosomal dominant inheritance. This syndrome is characterized by multiple odontogenic keratocysts, along with congenital skeletal anomalies and basal cell carcinomas. A 16-year-old girl was admitted with a complaint of swelling on the lower jaw. She had multiple basal cell nevi on both hands. Multiple lytic bone lesions on radiographs were defined as odontogenic keratocysts following the biopsy. The patient was referred to the Department of Physical Medicine and Rehabilitation for detailed musculoskeletal evaluation. Adam's forward bend te...
Source: The Turkish Journal of Pediatrics - July 1, 2014 Category: Pediatrics Authors: Keçeli O, Coskun-Benlidayı İ, Benlidayı ME, Erdoğan Ö Tags: Turk J Pediatr Source Type: research

The recurrence of odontogenic keratocysts in pediatric patients is associated with clinical findings of Gorlin-Goltz Syndrome.
CONCLUSION: Although uncommon in pediatric patients, OKC should be considered a differential diagnosis in cases of osteolytic lesions in gnathic bones. Thus, the periodic assessment of children by dentists and pediatricians is essential to get a correct diagnosis and early treatment to avoid greater mutilation of these patients. PMID: 31880290 [PubMed - as supplied by publisher]
Source: Medicina Oral, Patologia Oral y Cirugia Bucal - December 28, 2019 Category: ENT & OMF Tags: Med Oral Patol Oral Cir Bucal Source Type: research

A novel PTCH1 gene mutation in a pediatric patient associated multiple keratocystic odontogenic tumors of the jaws and Gorlin-Goltz syndrome.
This report documents a case of GGS with a novel mutation in the PTCH1 gene in an 11-year-old child. The clinical, radiographic, histopathologic and molecular findings of this condition, and treatment are described, and a review of GGS was carried out. PMID: 27510672 [PubMed - in process]
Source: Indian Journal of Pathology and Microbiology - June 30, 2016 Category: Pathology Authors: Ozcan G, Balta B, Sekerci AE, Etoz OA, Martinuzzi C, Kara O, Pastorino L, Kocoglu F, Ulker O, Erdogan M Tags: Indian J Pathol Microbiol Source Type: research

Genetic mutations in Gorlin-Goltz syndrome
This article presents a case of Gorlin-Goltz syndrome, its genetic predisposition, diagnosis and management.
Source: Indian Journal of Human Genetics - October 30, 2013 Category: Genetics & Stem Cells Authors: Muthumula DaneswariMutjumula Swamy Ranga Reddy Source Type: research

Gorlin Goltz syndrome: A case report
Publication date: Available online 26 February 2015 Source:International Journal of Dental Science and Research Author(s): Mahesh Chander , Madan Mishra , Amit Gaur , Tasveer Fatima , Shubhamoy Mondal , Shishir Dhar Not many cases have been reported in India, and hence we report here a rare case of Gorlin Goltz syndrome (GGS) especially in young patients without any skin lesions. A 21 year old male reported to our department, with swelling in the lower posterior region of the right side of jaw since last 2 years. Thorough extraoral and intraoral examinations along with orthopantomogram (OPG), CT scan (skull) and chest ra...
Source: International Journal of Dental Science and Research - February 27, 2015 Category: Dentistry Source Type: research

Meier-Gorlin syndrome
(MGS) is a rare autosomal recessive primordial dwarfism disorder, characterized by microtia, patellar applasia/hypoplasia, and a proportionate short stature. Associated clinical features encompass feeding problems, congenital pulmonary emphysema, mammary hypoplasia in females and urogenital anomalies, such as cryptorchidism and hypoplastic labia minora and majora. Typical facial characteristics during childhood comprise a small mouth with full lips and micro-retrognathia. During ageing, a narrow, convex nose becomes more prominent. The diagnosis MGS should be considered in patients with at least two of the three features ...
Source: Orphanet Journal of Rare Diseases - September 17, 2015 Category: Internal Medicine Authors: Sonja de MunnikElisabeth H. HoefslootJolt RoukemaJeroen SchootsNine KnoersHan BrunnerAndrew JacksonErnie Bongers Source Type: research

Gorlin-Goltz Syndrome: Report of Two Cases From the Same Family
Gorlin-Goltz syndrome, a hereditary autosomal dominant disorder characterized by multiple odontogenic keratocysts and basal cell carcinoma, may exhibit muscle, bone, neurologic, and endocrine alterations. A 45-year-old woman was referred by the genetic department for oral evaluation. An extra-oral examination showed multiple scars on the face; the patient reported the removal of several basal cell carcinomas. The panoramic radiograph revealed a unilocular radiolucent lesion in the right mandibular body.
Source: Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics - September 1, 2018 Category: ENT & OMF Authors: Gabriela Alacarini Farina, Carolina Dummel, Julia Turra Ribeiro, Stefanie Thieme Perotto, Andressa Cristina Hashigushi De Almeida, Marina Girardi Schueigart, Marco Antonio Trevizani Martins Tags: Oral and Maxillofacial Pathology Source Type: research

Gorlin-goltz syndrome: a report of two clinical cases with diagnosis and treatment at hospital level
Gorlin-Goltz syndrome, also known as nevoid basal cell carcinoma syndrome, is a rare hereditary autosomal dominant condition, with high penetrance and variable expressivity. The aim of this study is to report 2 cases diagnosed at emergency hospital units with the specialty of maxillofacial surgery and traumatology. The first refers to a 10-year-old patient who sought consultation due to an expressive increase in the maxilla volume with panoramic radiography evidencing multiple unilocular radiolucent images in the gnathic bones.
Source: Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics - August 17, 2022 Category: ENT & OMF Authors: Kelly Tambasco Bezerra, Gabriela Later ça Da Silva Abreu, Jackeline Nogueira De Paula Barros, Regina Celia De Souza Jesus Rangel, Alexandre Moreira De Moraes, Fábio Ramôa Pires, Águida Maria Menezes Aguiar Miranda Source Type: research

Diagnosis of gorlin-goltz syndrome: clincial case report
The diagnosis of Gorlin-Goltz syndrome involves clinical, radiographic, and histopathological aspects. Computed tomography contributes to the evaluation of the characteristics, to the extension of cystic lesions, and to the diagnosis of signs, such as calcifications in the falx cerebri. A 22-year-old male presented a complaint of halitosis. Upon extraoral examination, a slight increase in volume in the lower third of the right face, suggestive of a cystic lesion in the soft tissue, and a scar on the skin of the nasolabial region, were noted.
Source: Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics - June 15, 2023 Category: ENT & OMF Authors: Thiago Henrique Gon çalves MOREIRA, Regina Garcia DORTA, Mariana Quirino Silveira SOARES, Renata Hinhug Vilarinho CURADO, Daniela Carvalho TOSIN, José Luiz Cintra JUNQUEIRA, Vera Cavalcanti de ARAÚJO Source Type: research

Multiphase preclinical assessment of a novel device to locate unintentionally retained surgical sharps: a proof-of-concept study
CONCLUSIONS: The use of MSF in this study's RSS models facilitated the determination of presence and localization of RSS as shown by the increased rate of identification of a needle, decreased time to identification and higher accuracy in determining the presence of a needle. This device may be used in conjunction with radiography as it gives live visual and auditory feedback for users during the search for RSS.PMID:37101230 | DOI:10.1186/s13037-023-00359-8
Source: Patient Safety in Surgery - April 26, 2023 Category: Surgery Authors: Hae Sung Kang Jad Khoraki Jessie Gie Dielle Duval Susan Haynes Michael Siev Jay Shah Fernando Kim Martin Mangino Levi Procter Riccardo Autorino Samuel Weprin Source Type: research