Results 1 to 10 of about 727 (143)

Congenital radioulnar synostosis [PDF]

open access: yesRadiology Case Reports, 2017
Congenital radioulnar synostosis is a rare disorder resulting in the fusion of the radius and ulna from birth. Management is conservative. Operative treatment rarely succeeds.
Jeffrey Tsai, MBBS, FRACP
doaj   +8 more sources

Congenital Radioulnar Synostosis Review: Recommendations and Treatment Outcomes [PDF]

open access: yesChildren
Background/Objectives: Congenital radioulnar synostosis (CRS) is a rare congenital disorder of the elbow joint caused by the abnormal fusion of the radius and ulna during fetal development, leading to limited forearm rotation and functional impairment ...
Sergi Alabau-Rodriguez   +5 more
doaj   +7 more sources

Quantitative Analysis of Deformity in Digital Model of Congenital Radioulnar Synostosis [PDF]

open access: yesOrthopaedic Surgery, 2023
Objective The deformity of congenital radioulnar synostosis is quite complicated and difficult. This study aims to find out the related factors of the “forearm rotation angle” (FR) which relate to the severity of congenital radioulnar synostosis (CRUS ...
Chen Yang   +4 more
doaj   +3 more sources

Treatment of Congenital Radioulnar Synostosis Using a Free Vascularized Fascia Lata Graft [PDF]

open access: yesOrthopaedic Surgery, 2022
Objective To describe the modified mobilization surgery technique that uses a free vascularized fascia lata graft as the interposition graft, and to evaluate the outcome of this procedure in treating congenital radioulnar synostosis (CRUS).
Fan Bai   +9 more
doaj   +3 more sources

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   +5 more sources

Functional Assessment of Congenital Radioulnar Synostosis in Children [PDF]

open access: yesAvicenna Journal of Medicine
Background Congenital radioulnar synostosis (CRUS) is a rare condition caused by segmentation failure in embryonic life. The forearm is usually fixed in pronation, affecting the upper limb and hand functions.
Isam Sami Moghamis   +6 more
doaj   +4 more sources

Congenital radioulnar synostosis presenting in adulthood - a case report [PDF]

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   +5 more sources

Derotational osteotomy of the proximal radius and the distal ulna for congenital radioulnar synostosis [PDF]

open access: yesJournal of Children's Orthopaedics, 2008
Objective To evaluate the clinical and functional results of a technical procedure in the surgical treatment of congenital radioulnar synostosis in children. Materials and methods A prospective study had been undertaken from January 1992 to December 2004.
Nguyen Ngoc Hung
doaj   +3 more sources

Fracture of the two forearm bones and congenital radioulnar synostosis: A case report and review of literature [PDF]

open access: yesSAGE Open Medical Case Reports, 2023
Congenital proximal radioulnar synostosis limits prono-supination and is often well tolerated. Only one publication in the literature describes a fracture associated with this malformation. We report a case of radius and ulna shaft fractures in a 35-year-
Yassine Saadi   +2 more
doaj   +2 more sources

Congenital radioulnar synostosis: is prenatal diagnosis possible? - A case report

open access: yesTaiwanese Journal of Obstetrics & Gynecology, 2023
Objectives: The main objectives of this case report are to discuss prenatal ultrasound findings of congenital radioulnar synostosis and to review the literature.
Yi-Ying Li   +4 more
doaj   +3 more sources

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