Results 61 to 70 of about 732 (143)

Surgical outcome of delayed presentation of congenital proximal radioulnar synostosis

SICOT-J, 2015
Background: Presentation of proximal radioulnar synostosis varies from cosmetic concerns with no functional limitations to significant pronation deformity which hampers activities of daily living.
Garg Gaurav, Gupta Som P.
doaj   +1 more source

De Novo Interstitial Deletion of Chromosome 2 (p23p24)

Pediatrics and Neonatology, 2011
Structural anomalies associated with partial 2p monosomy are rare. There has only been one case of interstitial deletion of 2p24.2–2p25.1 and three cases of 2p23.3–2p25.1 described in the literature.
Pen-Hua Su, Jia-Yuh Chen, Teng-Fu Tsao, Suh-Jen Chen   +3 more
doaj   +1 more source

MEDICAL IMAGING AND 3D RECONSTRUCTION FOR OBTAINING THE GEOMETRICAL AND PHYSICAL MODEL OF A CONGENITAL BILATERAL RADIO-ULNAR SYNOSTOSIS [PDF]

Applied Computer Science, 2018
The paper presents results of a 3D reconstruction of a congenital bilateral radio-ulnar synostosis. Basics of anatomy and biomechanical analysis of the elbow joint were introduced.
Robert KARPIŃSKI, Józef JONAK, Jacek MAKSYMIUK   +2 more
doaj   +1 more source

Minimally invasive single-session double-level rotational osteotomy of the forearm bones to correct fixed pronation deformity in congenital proximal radioulnar synostosis

Journal of Children's Orthopaedics, 2016
Background Congenital proximal radioulnar synostosis is the most common congenital disease of the elbow joints and forearms. Methods This was a prospective study of 12 consecutive children (14 forearms) who presented to the National Institute of ...
Sherif N. G. Bishay
doaj   +1 more source

Four Cases of the Congenital Radioulnar Synostosis

Orthopedics & Traumatology, 1977
Recently we have experienced 4 patients of the congenital radioulnar synostosis.3 cases were bilateral radioulnal synostosis and 1 case was unilateral.2 of the bilateral cases were treated by method of resecting their radial head and fixing their forearms in supination with a kirschner wire and a screw.Postoperatively 2 patients have been improved ADL.
Kiyota, Y., Naono, T., Makino, T., Beppu, Y., Miyamoto, M., Nakamura, M.   +5 more
openaire   +2 more sources

Correction of deformities and length discrepancies of the forearm in children by distraction osteogenesis

Acta Orthopaedica et Traumatologica Turcica, 2021
Objectives: To review the results of correction of deformities and length discrepancies of the forearm in children. \r\nMethods: We evaluated the results of distraction osteogenesis in 10 forearms of nine patients with forearm shortening and/or deformity.
A. Erdem Bagatur, Ahmet Dogan, Gazi Zorer   +2 more
doaj  

A novel missense mutation in the MECOM gene in a Chinese boy with radioulnar synostosis with amegakaryocytic thrombocytopenia

BMC Pediatrics
Radioulnar synostosis with amegakaryocytic thrombocytopenia (RUSAT) type 2, caused by MDS1 and EVI1 complex locus (MECOM) gene mutations, is a rare inherited bone marrow failure syndrome (IBMFS) with skeletal anomalies, characterized by varying ...
Duowen Huang, Mingyan Jiang, Yiping Zhu, Dongjun Li, Xiaoxi Lu, Ju Gao   +5 more
doaj   +1 more source

Klippel–Feil Syndrome with Sprengel Deformity and Extensive Upper Extremity Deformity: A Case Report and Literature Review

Case Reports in Orthopedics, 2018
Introduction. Klippel–Feil syndrome (KFS) is a congenital anomaly resulting from fusion of cervical vertebral bodies secondary to the dysregulation of signaling pathways during somite development.
John W. Stelzer, Miguel A. Flores, Waleed Mohammad, Nathan Esplin, Jonathan J. Mayl, Christopher Wasyliw   +5 more
doaj   +1 more source

Congenital Radioulnar Synostosis: A Case Report and Review of Various Osteotomies. [PDF]

J Orthop Case Rep, 2023
Mehta G, Agrawal T, Jain D, Singh S.
europepmc   +1 more source

Rotational osteotomy with single incision and elastic fixation for congenital radioulnar synostosis in children: a retrospective cohort study. [PDF]

Transl Pediatr, 2022
Tan W, Yuan Z, Lin Y, Li Y, Ji Y, Sun Y, Xie D.   +6 more
europepmc   +1 more source