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Triorchidism diagnosed during a routine hernia repair: A case report and literature review.
Int J Surg Case Rep
December 2024
Department (B) of Visceral Surgery, Charles Nicolle Hospital, Tunis, Tunisia.
Introduction: Triorchidism is a rare anomaly whose management raised considerable discussion. Several factors must be considered, including the patient's age, the testes location, their functional status, and the accessibility and compliance for follow-up. We present a case of triorchidism diagnosed incidentally during a routine hernioplasty procedure, serving educational and informative purposes.
View Article and Find Full Text PDFImpacted supernumerary tooth in the horizontal plate of palatine bone: a rare case report.
BMC Oral Health
December 2024
Nepalese Army Institute of Health Sciences, College of Medicine, Kathmandu, Nepal.
Background: Supernumerary teeth, defined as extra teeth beyond the normal series of dentition, can appear anywhere in the dental arch. They may present as solitary or multiple, unilateral or bilateral, and can be either erupted or impacted. Rarely, supernumerary teeth are found in ectopic locations outside the dental arches, such as the nasal cavity, inferior nasal conchae, maxillary sinus, ethmoid sinus, or skull.
View Article and Find Full Text PDFThe impact of RUNX2 gene variants on cleidocranial dysplasia phenotype: a systematic review.
J Transl Med
December 2024
Department of Physiology, Center of Excellence in Genomics and Precision Dentistry, Faculty of Dentistry, Chulalongkorn University, Bangkok, 10330, Thailand.
Cleidocranial Dysplasia (CCD) is a rare genetic disorder characterized by skeletal abnormalities and dental anomalies, primarily caused by variants in the RUNX2 gene. Understanding the spectrum of RUNX2 variants and their effects on CCD phenotypes is crucial for accurate diagnosis and management strategies. This systematic review aimed to comprehensively analyze the genotypic and phenotypic spectra of RUNX2 variants in CCD patients, assess their distribution across functional regions, and investigate genotype-phenotype correlations.
View Article and Find Full Text PDFCongenitally missing permanent canines in a sample of Chinese population: a retrospective study.
BMC Oral Health
November 2024
Department of Stomatology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, 100045, China.
Article Synopsis
- * After analyzing over 10,000 panoramic radiographs, researchers found a CMPC prevalence of 0.69%, with a notable difference between age groups: younger patients (under 10 years) had lower prevalence compared to older patients (ages 10 and above).
- * Most missing canines were found in the upper jaw, with a significant majority of patients having visible primary canines; additional anomalies like other missing teeth and microdontia were also noted among affected individuals.
Comprehensive Management of an Impacted Maxillary Central Incisor: A Case Report.
Cureus
October 2024
Pediatric Dentistry, Manav Rachna Dental College, School of Dental Sciences, Faridabad, IND.
The impaction of a maxillary central incisor in young patients is rare but can significantly affect aesthetics, speech, and self-esteem. This case report details the diagnosis and treatment of an 11-year-old male patient with an impacted maxillary right central incisor, along with the presence of an impacted supernumerary tooth (mesiodens). The case was managed through a combination of surgical exposure of the impacted tooth and orthodontic traction to guide the impacted tooth into its correct position.
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