Results 11 to 20 of about 40,078 (160)
The Egyptian Journal of Radiology and Nuclear Medicine, 2021 Background Klippel-Feil syndrome (KFS) is a congenital malformation causing fusion of at least two cervical vertebrae and characterized clinically by presence of triad of short neck, limited neck movements, and low posterior hair line.
Mohammad Shoaib +2 more
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Asymmetric skeletal anomalies in siblings [PDF]
Clinical Genetics, 1984 We describe two siblings with asymmetric limb reduction malformations. Such anomalies are usually considered to result from sporadic events, but the recurrence in siblings without any identifiable teratogenic insult suggests a genetic etiology. This finding becomes important when parents are counseled about future pregnancies.
Stanley, Wayne S. +5 more
openaire +3 more sources
Journal of Orthodontic Science, 2022 OBJECTIVE: The main objective of this study is to get a wider and clearer idea about the relationship between sella turcica bridging and the type of dental anomalies related to size, shape, number, structure and eruption of teeth.
Priyanka C Saokar +2 more
doaj +1 more source
Dental anomalies in orthodontic patients with and without skeletal discrepancies
Dentistry 3000, 2020 Objective:To determine whether individuals withskeletal discrepancies of Class II or IIIdisplay a higher frequency of dental anomalies in comparison with individuals with Class I malocclusion.
Clarissa Christina Avelar Fernandez +3 more
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BMC Oral Health, 2023 Introduction Despite researchers' recent interest in identifying links between some dental and craniovertebral abnormalities, there are many important, unassessed gaps in our knowledge of this matter. In addition, previous samples were small.
Farhad Sobouti +3 more
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Anaesthetic considerations in an orphan disease with skeletal anomalies.
Indian J Anaesth, 2016 Datta R, Agarwal J, Sharma DK.
europepmc +4 more sources
Frontiers in Genetics, 2023 FOXC1 is a ubiquitously expressed forkhead transcription factor that plays a critical role during early development. Germline pathogenic variants in FOXC1 are associated with anterior segment dysgenesis and Axenfeld-Rieger syndrome (ARS, #602482), an ...
Alexandra Garza Flores +26 more
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Applied Sciences, 2020 This study aims to evaluate whether or not there is a higher prevalence of skeletal abnormalities in subjects with maxillary canine impaction (MCI). This retrospective study was performed on 67 subjects with maxillary canine impaction (test group) and on
Marco Pasini +6 more
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Early prenatal diagnosis of skeletal anomalies [PDF]
Prenatal Diagnosis, 2011 AbstractObjectiveTo review experience of early prenatal diagnosis of skeletal dysplasias, and to explore diagnostic accuracy and improve management.MethodsA retrospective review of fetal medicine unit (FMU) records was performed to identify cases where a skeletal dysplasia was suspected by 14 weeks' gestation.
Khalil, Asma +2 more
openaire +3 more sources
Recurrent Urinary Tract Infection as a Manifestation of Goldenhar Syndrome: Case Report
Van Tıp Dergisi, 2019 Goldenhar syndrome is a rare disease characterized by anomalies of the ear, eye and vertebrae, caused by developmental failure of the first and second brachial arches. Genitourinary, cardiac, skeletal and central nervous system anomalies can also be seen
Ali Güngör +5 more
doaj +1 more source