Results 21 to 30 of about 727 (143)

Derotational Osteotomy and Plate Fixation of the Radius and Ulna for the Treatment of Congenital Proximal Radioulnar Synostosis

Frontiers in Surgery, 2022
PurposeTo evaluate the clinical outcomes of derotational osteotomy followed by plate fixation at the radius and ulna for the treatment of congenital proximal radioulnar synostosis.MethodsA total of 10 eligible patients (12 forearms) with congenital ...
Yimurang Hamiti, Maimaiaili Yushan, Ainizier Yalikun, Cheng Lu, Aihemaitijiang Yusufu   +4 more
doaj   +3 more sources

Molecular Landscape in Limb Anomalies: Diagnostic Yield and New Candidate Genes. [PDF]

Clin Genet
In 132 individuals with limb anomalies, diagnostic yield was 36% (47/132), including 25 novel variants, three cases with new phenotypes, and two candidate loci, HOXA11 and a small 2q31.1 deletion. Mouse data and exome‐wide analysis, key in identifying the candidate loci, represent an important opportunity for gene discovery.
Mokhtari A, Charbonneau J, Miranda V, Jizi K, Delrue MA, Egerszegi P, Thiffault I, Campeau PM.   +7 more
europepmc   +2 more sources

A dual dimensional optimization strategy for automatic osteotomy preoperative planning in congenital radioulnar synostosis [PDF]

Scientific Reports
Congenital radioulnar synostosis (CRUS) presents a complex forearm deformity, requiring precise osteotomy planning for anatomical restoration. This study proposes an automatic osteotomy preoperative planning method for forearms with CRUS.
Ying Cui, Tianfeng Zhou, Yubing Guo, Xinhua Zhou, Lu Liu, Shanlin Chen   +5 more
doaj   +2 more sources

Dynamic sonographic diagnosis of snapping elbow associated with congenital radioulnar synostosis [PDF]

JSES Reviews, Reports, and Techniques, 2023
Kensuke Kameda, MD, Kazuma Miyatake, MD, PhD, Takahiro Fujisawa, MD, Akio Otoshi, MD, Yusuke Kawabata, MD, PhD, Yohei Kusaba, MD, Yutaka Inaba, MD, PhD   +6 more
doaj   +2 more sources

Outcomes of derotation osteotomy at synostosis site for congenital radioulnar synostosis

PAMJ Clinical Medicine, 2019
Congenital radioulnar synostosis (CRUS) is rare upper limb malformation in which proximal portions of the radius and ulna fuse with each other and restricts the rotation of the forearm.
Tazi Charki Mohammed, Abdellaoui Hicham, Atarraf Karima, Chater Lamyae, Afifi Moulay-Abderahman   +4 more
doaj   +2 more sources

Traumatic elbow dislocation in a patient with congenital radioulnar synostosis [PDF]

Shoulder and Elbow, 2022
Alexander Barclay
exaly   +2 more sources

An automatic congenital radio-ulnar synostosis deformity evaluation method (CRUS-DE): integrating TLT-SAM and GPMM-R for landmark identification [PDF]

Scientific Reports
Congenital Radio-Ulnar Synostosis (CRUS) causes difficulty in forearm rotation, which is treated using osteotomy. Effective preoperative planning of osteotomy requires automatic and objective quantification of deformity angles.
Lu Liu, Ying Cui, Tianfeng Zhou, Shanlin Chen, Yubing Guo, Xinhua Zhou   +5 more
doaj   +2 more sources

Congenital Radioulnar Synostosis

Journal of the American Academy of Orthopaedic Surgeons, 2021
Congenital radioulnar synostosis is a rare condition resulting in fusion of the proximal portions of the radius and ulna. Patients commonly present in early childhood with functional deficits because of limited forearm rotation and fixed positioning of the forearm. Compensatory motion and hypermobility are frequently observed at the wrist and shoulder,
Paul T. Rutkowski, Julie Balch Samora
  +5 more sources

Measurement of compensatory wrist joint rotation using three-dimensional motion analysis in patients with unilateral proximal congenital radioulnar synostosis [PDF]

Acta Orthopaedica et Traumatologica Turcica, 2021
Qingyuan Li, Jay Hoon Park, Yohan Lee, Jihyeung Kim, Kee Jeong Bae, Goo Hyun Baek   +5 more
doaj   +2 more sources

Pathogenic SMAD6 variants in patients with idiopathic and complex congenital heart disease associated pulmonary arterial hypertension [PDF]

npj Genomic Medicine
In patients with complex congenital heart disease (CHD) pathogenic SMAD6 variants have been described previously. The aim of this study was to analyze if pathogenic SMAD6 variants also occur in patients with CHD associated with pulmonary arterial ...
Sofia Karl, Ekkehard Grünig, Memoona Shaukat, Matthias Held, Christian Apitz, Fabian von Scheidt, Ralf Geiger, Michael Halank, Karen M. Olsson, Marius M. Hoeper, Jan C. Kamp, Gabor Kovacs, Horst Olschewski, Hans-Jürgen Seyfarth, Katrin Milger, Ralf Ewert, Hans Klose, Benjamin Egenlauf, Panagiota Xanthouli, Katrin Hinderhofer, Christina A. Eichstaedt   +20 more
doaj   +2 more sources