Results 21 to 30 of about 5,517 (177)

Prevalence and Morphological Characteristics of Occipito-Atlanto-Axial Fusion among South Indian Population: A Cross-sectional Study [PDF]

open access: yesInternational Journal of Anatomy Radiology and Surgery
Introduction: The anatomy of the cervical vertebrae, along with the atlanto-occipital joint, allows for free flexion, extension and rotation, which occurs almost entirely in the first two cervical vertebrae.
Khushali Rai, Sharada B Menasinkai
doaj   +1 more source

Rare complication of open reduction and internal fixation of fracture distal radius

open access: yesTrauma Case Reports, 2022
Case: A 57-years old man who sustained left distal radius fracture. We performed distal radius ORIF. At follow up visit, he could not achieve any supination-pronation movements. Radiographs showed radioulnar synostosis.
Ahmed Elmahdi   +2 more
doaj   +1 more source

Metopic synostosis [PDF]

open access: yesChild's Nervous System, 2012
Premature closure of the metopic suture results in a growth restriction of the frontal bones, which leads to a skull malformation known as trigonocephaly. Over the course of recent decades, its incidence has been rising, currently making it the second most common type of craniosynostosis.
openaire   +2 more sources

Radiographic Assessment of Congenital C2–3 Synostosis

open access: yesJournal of Orthopaedic Surgery, 2010
Purpose. To evaluate the morphologies of congenital C2–3 synostosis in 25 patients. Methods. Radiographs of 11 males and 14 females aged 5 to 74 years with congenital C2–3 synostosis were reviewed.
Myung-Sang Moon   +5 more
doaj   +1 more source

SURGICAL TREATMENT OF METACARPAL SYNOSTOSIS IN CHILDREN

open access: yesTravmatologiâ i Ortopediâ Rossii, 2012
Objective: to develop the surgical treatment of patients with congenital metacarpal synostosis. Material and methods. 65 operations were performed in 58 children. with congenital metacarpal synostosis.
A. V. Zaletina
doaj   +1 more source

Congenital Humeroradial Synostosis: A Case Report [PDF]

open access: yesMalaysian Orthopaedic Journal, 2012
We present here a unique case of humeroradial synostosis. These anomalies are due to longitudinal failure of differentiation. Approximately 150 cases of humeroradial synostosis have been reported worldwide, the majority of which are familial in nature or
Sandeep Nema   +3 more
doaj   +1 more source

Complete Maxillo-Mandibular Syngnathia in a Newborn with Multiple Congenital Malformations

open access: yesPediatrics and Neonatology, 2016
Syngnathia is an extremely rare condition involving congenital fusion of the maxilla with the mandible. Clinical presentations vary from simple mucosal bands (synechiae) to complete bony fusion (synostosis).
M. Broome   +5 more
doaj   +1 more source

Congenital proximal radioulnar synostosis—a case report

open access: yesRadiology Case Reports, 2020
Congenital radioulnar synostosis is a rare anomaly of the forearm with restrictions of full movement of the affected limbs. It is often seen in early childhood when they present with functional impairments.
Iseko Kingsley Iyoko, MBBS(Ib), FWACS   +3 more
doaj   +1 more source

QS3: Influence Of Nonsyndromic Bicoronal Synostosis And Syndromic Influences On And Periorbital Malformation

open access: yesPlastic and Reconstructive Surgery, Global Open, 2021
Background Oculo-orbital disproportion in patients with craniosynostosis have similarities and dissimilarities between syndromic and nonsyndromic cases. We hypothesize these two conditions have specific individual influences as it relates to development ...
Xiaona Lu, MD, PhD   +4 more
doaj   +1 more source

Congenital radioulnar synostosis presenting in adulthood - a case report

open access: yesThe Pan African Medical Journal, 2020
Congenital radioulnar synostosis is a rare developmental skeletal malformation of the upper limb, characterized by the fusion of the proximal ends of the radius and ulna from birth. The failure of prenatal longitudinal segmentation of the adjacent radius
Mohammed Hamid Karrar Alsharif   +6 more
doaj   +1 more source

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