Background/objectives: This study aimed to investigate the prevalence and characteristics of positional anomalies in second permanent molars among Romanian patients. These molars play a crucial role in occlusion but can exhibit positional issues such as tilting, rotation, infraocclusion, and impaction.
Methods: This retrospective study examined the digital models of 103 patients aged 12-40, which were obtained by using the Medit i500 intraoral scanner. Positional anomalies were categorized by tilting, rotation, infraocclusion, and impaction.
Results: The results showed a high prevalence of anomalies, particularly infraocclusion and buccal tilting in upper molars and oral tilting and mesio-buccal rotations in lower molars. The significant symmetry of anomalies within the same dental arch was noted. Gender and malocclusion type did not significantly influence anomaly frequency.
Conclusions: The findings emphasize the need for the vigilant monitoring of second permanent molars to maintain functional occlusion and suggest potential common etiological factors within dental arches. Despite this study's limitations, including sample size and retrospective design, this study underscores the clinical importance of the early detection and management of molar anomalies. Future research should expand on these findings, considering genetic and environmental influences on dental development.
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http://dx.doi.org/10.3390/pediatric16040097 | DOI Listing |
Pediatr Rep
December 2024
Department of Dentistry, Faculty of Medicine and Pharmacy, University of Oradea, 410073 Oradea, Romania.
Background/objectives: This study aimed to investigate the prevalence and characteristics of positional anomalies in second permanent molars among Romanian patients. These molars play a crucial role in occlusion but can exhibit positional issues such as tilting, rotation, infraocclusion, and impaction.
Methods: This retrospective study examined the digital models of 103 patients aged 12-40, which were obtained by using the Medit i500 intraoral scanner.
Preduodenal portal vein (PDPV) is a rare congenital vascular malformation, which was first described by Knight in 1921 as an anomalous vein that lies in front of the duodenum, common bile duct, and hepatic artery instead of beneath them. This abnormal position may result in congenital duodenal obstruction and puts it in danger during operations around this region. PDPV is typically associated with other congenital anomalies, mainly intraabdominal and cardiac ones.
View Article and Find Full Text PDFJ Mov Disord
December 2024
Graduate School of Health Sciences, Kio University, Nara, Japan.
Objective: Camptocormia has been considered to contribute to vertical gait instability and, at times, may also lead to forward instability in experimental settings in Parkinson's disease (PD). However, these aspects, along with compensatory mechanisms, remain largely unexplored. This study comprehensively investigated gait instability and compensatory strategies in PD patients with camptocormia (PD+CC).
View Article and Find Full Text PDFFront Neurol
December 2024
Department of Neurology, Dongzhimen Hospital Affiliated to Beijing University of Chinese Medicine, Beijing, China.
Objective: The objective of the study is to analyze and explore the characteristics of the video head impulse test (vHIT) for light cupula in the idiopathic horizontal semicircular canal and compare them with those of horizontal semicircular canal cupulolithiasis (HC-cu) in order to investigate the potential mechanism involved.
Methods: Data from 51 cases of idiopathic light cupula and 42 cases of horizontal semicircular canal cupulolithiasis were retrospectively analyzed. The positional nystagmus features, vHIT anomaly rate, gain value, saccades, and other indicators were compared.
Expert Rev Respir Med
December 2024
Division of Thoracic Surgery, Department of Surgery, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Introduction: Situs inversus is a rare congenital condition where the organs in the chest and abdomen are reversed, thus complicating surgeries such as lung transplantation. Kartagener syndrome (KS), associated with situs inversus, includes chronic sinusitis and bronchiectasis, which can progress to end-stage lung disease requiring transplantation. This review discusses the unique surgical considerations, technical challenges, and outcomes of lung transplantation in patients with situs inversus, particularly KS.
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