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Micro-Computed Tomographic Analysis of the Mesial Root of Mandibular First Molars With Bifid Apex
Archives of Oral Biology, 2020 Objectives: The aim of the present study was to evaluate the influence of bifid and non-bifid configurations of the mesial root of mandibular first molars in the canal anatomy using micro-computed tomography (micro-CT)
Marco Aurélio Versiani +2 more
exaly +2 more sources
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International Journal of Pediatric Otorhinolaryngology, 1999
Bifid epiglottis is a rare congenital defect that is often associated with other congenital annomalies. The most common defect associated with a bifid epiglottis are anomalies of the hands and/or feet (90%) while the most dangerous and potentially lethal anomaly if not recognized and treated are hypothalamic hamartomas and hypopituitarism (50%).
Frank L Rimell
exaly +3 more sources
Bifid epiglottis is a rare congenital defect that is often associated with other congenital annomalies. The most common defect associated with a bifid epiglottis are anomalies of the hands and/or feet (90%) while the most dangerous and potentially lethal anomaly if not recognized and treated are hypothalamic hamartomas and hypopituitarism (50%).
Frank L Rimell
exaly +3 more sources
Prevalence of Bifid Uvula in Primary School Children
International Journal of Pediatric Otorhinolaryngology, 2019 A bifid uvula is an anatomic variation that can be predictive of sub-mucous cleft palate, which may cause velopharyngeal insufficiency (VPI). Bifid uvula prevalence in the literature ranges from 0.18% to 10.3%, depending on the population studied.
Giorgio La Scala, Igor Leuchter
exaly +2 more sources
Significance of Bifid Epiglottis
American Journal of Medical Genetics, Part A, 2005AbstractBifid epiglottis is a rare anomaly, which is heterogeneous and is often associated with other anomalies, particularly polydactyly. It has been reported in 40% of patients with Pallister–Hall syndrome and rarely in other syndromes. We report two brothers with bifid epiglottis who also have features suggestive of Bardet–Biedl syndrome.
Cathy A Stevens
exaly +3 more sources
The Laryngoscope, 1972
AbstractSeemingly minor anatomical variants may herald more serious and complicated anatomical or physiological abnormalities. A white forelock is present in 20 percent of cases with Waardenburg's syndrome. Blue sclera suggests the diagnosis of otosclerosis or osteogenesis imperfecta.
openaire +4 more sources
AbstractSeemingly minor anatomical variants may herald more serious and complicated anatomical or physiological abnormalities. A white forelock is present in 20 percent of cases with Waardenburg's syndrome. Blue sclera suggests the diagnosis of otosclerosis or osteogenesis imperfecta.
openaire +4 more sources
Annals of Otology, Rhinology & Laryngology, 1996
The true bifid epiglottis is a rare congenital anomaly typically discovered during the evaluation of stridor in an infant or newborn. While it is not classified as a specific syndrome, there are frequent associations of other congenital anomalies with the bifid epiglottis.
J D, Goldenberg +3 more
openaire +2 more sources
The true bifid epiglottis is a rare congenital anomaly typically discovered during the evaluation of stridor in an infant or newborn. While it is not classified as a specific syndrome, there are frequent associations of other congenital anomalies with the bifid epiglottis.
J D, Goldenberg +3 more
openaire +2 more sources
Journal of Oral and Maxillofacial Surgery, 2003
To determine the incidence and characteristics of bifid mandibular canals.A retrospective study was performed using panoramic radiographs of 2012 patients subjected to dental treatment in the Dental Clinic of the Valencia University Dental School (Valencia, Spain) between 1996 and 1999.
J M, Sanchis +2 more
openaire +2 more sources
To determine the incidence and characteristics of bifid mandibular canals.A retrospective study was performed using panoramic radiographs of 2012 patients subjected to dental treatment in the Dental Clinic of the Valencia University Dental School (Valencia, Spain) between 1996 and 1999.
J M, Sanchis +2 more
openaire +2 more sources
Acta Orthopaedica Scandinavica, 1976
Two identical and unusual cases of congenital bifid femur are described. Both cases were successfully rehabilitated after simple surgery and the fitting of a suitable prosthesis. The patients are now able to walk without any form of external support.
B, Aalami-Harandi, A, Zahir
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Two identical and unusual cases of congenital bifid femur are described. Both cases were successfully rehabilitated after simple surgery and the fitting of a suitable prosthesis. The patients are now able to walk without any form of external support.
B, Aalami-Harandi, A, Zahir
openaire +2 more sources