Results 51 to 60 of about 9,755 (160)

Prevalence of Different Types of the Bifid Mandibular Canal and its Relationship with the Position and Width of the Main Canal in the Panoramic Radiographs

open access: yesMajallah-i Dānishgāh-i ̒Ulūm-i Pizishkī-i Qum, 2020
Background and Objectives: The presence of bifid mandibular canals are among the anatomical variations in the inferior mandibular canals. Lack of attention to these canals can lead to complications, such as anesthesia and bleeding during dental ...
Mohammad Mehdizadeh   +3 more
doaj  

Bifid mandibular condyle: A rare disorder

open access: yes, 2006
Bifid mandibular condyle is a rare disorder and little is known about the etiology and pathogenesis. We reported a patient with left bifid mandibular condyle with a history of trauma.
Mavili, M. Emin   +2 more
core   +1 more source

Craniofacial development in patients of Tessier No.0 cleft with a bifid nose using 3D computed tomography

open access: yesFrontiers in Pediatrics, 2022
ObjectiveConsiderable studies have focused mainly on the facial deformity of Tessier No.0 cleft with a bifid nose, but the deformity of the skull is not well understood. Therefore, our study aimed to explore the evolution of cranial dysmorphology and the
Xin Wang   +5 more
doaj   +1 more source

Prolotherapy Perineural Injection in Carpal Tunnel Syndrome with Bifid Median Nerve: A Case Report

open access: yesJournal Orthopaedi and Traumatology Surabaya, 2022
Background: Carpal tunnel syndrome (CTS) is a common neuropathy condition caused by entrapment of  the median nerve. Perineural injection therapy with 5% dextrose or prolotherapy becoming a common method for treating carpal tunnel syndrome.
Tresna Angga Basunanda   +1 more
doaj   +1 more source

A Familial Case of Thauvin–Robinet–Faivre Syndrome (TROFAS), Presenting With Postaxial Polydactyly and Upper Lip Vascular Malformation

open access: yesClinical Genetics, EarlyView.
These two siblings carrying the homozygous FIBP c.412‐3_415dupCAGTTTG variant, previously identified in several Turkish families, further delineate the clinical spectrum of TROFAS. Postaxial polydactyly and an upper lip vascular malformation, observed in Patient 2, have not previously been reported in association with this syndrome.
Federica Ruscitti   +9 more
wiley   +1 more source

Bifid Pelvis Appearance and Y [PDF]

open access: yes, 2017
Bifid (two-compound) renal pelvis constitutes 10% of normal renal pelvis. The Yo-Yo reflux is reflux from one ureter to another in incomplete ureteral duplications. The diagnosis of yo-yo reflux is difficult. Technetium-99m diethylenetriamine pentaacetic
Araz, Mine, Cayir, Derya
core  

Bifid Throats for Axion Monodromy Inflation [PDF]

open access: yes, 2015
We construct a simple explicit local geometry providing a `bifid throat' for 5-brane axion monodromy. A bifid throat is a throat that splits into two daughter throats in the IR, containing a homologous 2-cycle family reaching down into each daughter ...
Ander Retolaza   +5 more
core   +1 more source

Prevalence of Bifid Median Nerve and the Cross-Sectional Area as Assessed by Ultrasonography in Healthy Japanese Subjects

open access: yesJournal of Hand Surgery Global Online, 2019
Purpose: Ultrasonography is useful for evaluating anatomical variations of the median nerve and aids in diagnosing carpal tunnel syndrome by assessing the cross-sectional area (CSA) at the carpal tunnel inlet.
Satoshi Shinagawa, MD   +10 more
doaj   +1 more source

Cerebral Ventriculomegaly With Abnormality of the Aqueduct of Sylvius: A Case Series

open access: yesClinical Genetics, EarlyView.
Genetic testing leads to a diagnostic rate of ~30% in a fetal cohort with cerebral ventriculomegaly where the neuropathological examination revealed a stenosis or atresia of the aqueduct of Sylvius. ABSTRACT Fetal cerebral ventriculomegalies are brain anomalies with potentially poor neurodevelopmental prognosis.
Romain Nicolle   +20 more
wiley   +1 more source

RLIM‐associated neurodevelopmental disorders: From clinical spectrum to molecular mechanisms

open access: yesThe FEBS Journal, EarlyView.
RLIM (RNF12) is an E3 ubiquitin ligase essential for mammalian development. Loss‐of‐function variants cause Tønne–Kalscheuer syndrome, while duplications cause Xq13 duplication syndrome, highlighting RLIM dosage sensitivity. This review summarizes the genetics, clinical features, and molecular mechanisms of RLIM‐associated disorders, integrating ...
Madison Landon   +4 more
wiley   +1 more source

Home - About - Disclaimer - Privacy