Results 11 to 20 of about 3,326,748 (262)

Recurrence rate after radial club hand surgery in long term follow up [PDF]

open access: yesJournal of Research in Medical Sciences, 2009
<ul><li><strong>BACKGROUND</strong>: Radial club hand includes wide spectrum of&nbsp; alformations that involve radial side of forearm.
hooman shariatzadeh   +3 more
doaj   +2 more sources

Operative treatment of the radial club hand

open access: yesActa Orthopaedica et Traumatologica Turcica, 2021
Eight patients with twelve congenital radial club hand deformities were treated by two different surgical methods. One of them was centralization of the ulna into the carpus and the transpozition of the flexor and extansor carpi radialis tendons to the ...
Ayan Gulgonen, Turker Ozkan, Ali Baktir
doaj   +1 more source

“Less is More”- A Minimalistic Surgical Intervention to Correct the Right Upper Limb Deformity in an Isolated Right Radial Club Hand: A Case Report [PDF]

open access: yesJournal of Orthopaedic Case Reports
Introduction: Radial club hand is a rare congenital condition (1 in 100,000) involving varying deformities on the radial side of the forearm, ranging from thumb underdevelopment to absence of the radius and related structures.
Sunil Kumar Rout   +3 more
doaj   +2 more sources

The Paley ulnarization of the carpus with ulnar shortening osteotomy for treatment of radial club hand [PDF]

open access: yesSICOT-J, 2017
Recurrent deformity from centralization and radialization led to the development in 1999 of a new technique by the author called ulnarization. This method is performed through a volar approach in a vascular and physeal sparing fashion. It biomechanically
Paley Dror
doaj   +2 more sources

Recurrence rate of radial deviation following the centralization surgery of radial club hand [PDF]

open access: yesMedical Journal of The Islamic Republic of Iran, 2018
Background: Congenital radial club hand (RCH), as a rare congenital deformity of the upper extremity, is characterized by a wide spectrum of malformations including radial deviation. Centralization surgery is the standard treatment for severe cases that have been associated with a high rate of recurrence.
Najd Mazhar, Farid   +4 more
openaire   +3 more sources

From Hope to Heartache: A Case Report of Treatment Failure and its Impact on a 1-year-old with Bilateral Radial Aplasia in a Resource-Limited Setting [PDF]

open access: yesJournal of Orthopaedic Case Reports
Introduction: Radial aplasia is a rare congenital anomaly of the upper limbs, more common in females, affecting between one in 30,000 and one in 100,000 live births, and primarily impacting structures on the radial side of the forearm.
Oluwatosin Gabriel Afolabi   +2 more
doaj   +2 more sources

Alteration of a radial forearm flap to adjust to the superficial radial artery: a case report [PDF]

open access: yes, 2022
Aberrant branches of the radial artery at the level of the forearm have rarely been reported. Preoperative workups to identify aberrant branches of this type have also seldom been performed.
서영철
core   +1 more source

Bilateral Finger Morton Neuroma after Primary Fingertip Amputation

open access: yesPlastic and Reconstructive Surgery, Global Open, 2022
Summary:. Morton’s neuroma (MN) is a painful, proliferative fibrosis of perineural tissue caused by pressure or recurrent irritation that was previously thought to affect only the common interdigital nerve of the foot. We present a case of a bilateral MN
Adrian Georg Mogl   +4 more
doaj   +1 more source

Forearm lengthening: Management of elbow and wrist

open access: yesJournal of Children's Orthopaedics, 2016
The risk and consequences of an elbow or a wrist contracture are lower during a forearm lengthening than during a lower limb lengthening. This kind of complication can mostly be avoided by an active and intensive regimen of physiotherapy.
Franck Launay, Sébastien Pesenti
doaj   +1 more source

Radial, renal and craniofacial anomalies: Baller-Gerold syndrome

open access: yesIndian Journal of Plastic Surgery, 2008
The Baller-Gerold syndrome is a rare syndrome with very few cases published in literature. Craniosynostosis and radial aplasia are striking features, easy to diagnose. However, there are many differential diagnoses.
Jyotsna Murthy   +2 more
doaj   +3 more sources

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