Results 11 to 20 of about 48,690 (312)

Foot deformities and gait deviations in children with arthrogryposis

Journal of Limb Lengthening & Reconstruction, 2019
Objectives: Arthrogryposis multiplex congenita is a congenital condition characterized by joint contractures with resulting foot deformities and gait deviations.
Lucio Perotti, Chris Church, Celina Santiago, Nancy Lennon, John Henley, Kristen Nicholson, Jose Salazar-Torres, Maureen Donohoe, Kathryn Fazio, Freeman Miller, Louise Reid Nichols   +10 more
doaj   +2 more sources

Congenital Calcaneovalgus:With Special Reference to Treatment and its Relation to Other Congenital Foot Deformities [PDF]

Acta Orthopaedica Scandinavica, 1974
(1974). Congenital Calcaneovalgus: With Special Reference to Treatment and its Relation to Other Congenital Foot Deformities. Acta Orthopaedica Scandinavica: Vol. 45, No. 1-4, pp. 145-151.
B, Larsen, I, Reimann, H, Becker-Andersen   +2 more
openaire   +3 more sources

Defining and Differentiating Congenital Vertical Talus and Congenital Oblique Talus

JBJS Open Access
Background:. Congenital vertical talus (CVT) and congenital oblique talus (COT) are rocker-bottom foot deformities that have similar names and no objective definitions.
Vincent S. Mosca, MD, Dhiren Ganjwala, MS(Ortho), Hitesh Shah, MS(Ortho)   +2 more
doaj   +2 more sources

A re-examination of the patterns of foot and ankle deformities in congenital limb deficiencies

Journal of Limb Lengthening & Reconstruction, 2021
Purpose: The aim of this study is to evaluate foot deformities and anomalies present in congenital limb deficiencies (CLDs). We sought to define the relationship between the type of limb deficiency and foot posture, patterns of ray deficiencies, and ...
A. Kothari, S. Kelley, Maryse Bouchard
semanticscholar   +1 more source

Congenital Clubfoot - Is the Ponseti Method the Definitive Solution? [PDF]

Revista Brasileira de Ortopedia, 2022
Congenital clubfoot is one of the most common deformities at birth. The inadequacy or absence of treatment causes serious limitations for people with this condition.
Felippi Guizardi Cordeiro, Rodrigo Sousa Macedo, Bruno Sérgio Ferreira Massa, Patricia Moreno Grangeiro, Alexandre Leme Godoy-Santos, Túlio Diniz Fernandes   +5 more
doaj   +1 more source

COMPARISON BETWEEN TWO TYPES OF ABDUCTION ORTHOTICS IN TREATING CONGENITAL CLUBFOOT [PDF]

Acta Ortopédica Brasileira, 2017
Objective: The objective of this study was to analyze and compare the effectiveness of two types of abduction orthotics used for the feet, the Denis-Browne type (traditional) and the Dobbs type (dynamic), with regard to maintenance of deformity ...
Luiz Carlos Ribeiro Lara, Bruno Leite Gil, Lucio Carlos de Azevedo Torres Filho, Tarsila Pagnan Silva dos Santos   +3 more
doaj   +1 more source

Total ankle replacement for treatment of complex congenital fibular hemimelia

Foot & Ankle Surgery: Techniques, Reports & Cases, 2022
Fibular hemimelia is a rare congenital disorder of unknown etiology characterized by fibular hypoplasia, dysplasia, or complete aplasia. The pathologic process is occasionally associated with other femoral, tibial and/or foot deformities.
Cody J. Togher, DPM, AACFAS, John M. Thompson, DPM, AACFAS, Trevor S. Page, BS, Gregory C. Berlet, MD, FRCS(C), FAOA   +3 more
doaj   +1 more source

Development and Test of a Serious Game for Dorsiflexion and Plantarflexion Exercises of the Feet

Journal on Interactive Systems, 2021
Congenital clubfoot is the most common disease of the musculoskeletal system, causing deformities in the musculature of the foot and requiring long-term motor rehabilitation. This article shows the design and development of a serious game to support the
Daniel Rogério Ferreira, Caio Kaufman Baptista, Bruno da Silva Rodrigues, Barbara Campos Siqueira, Silvana M. Blascovi-Assis, Ana Grasielle Corrêa   +5 more
doaj   +1 more source

Caudal Regression Syndrome: A Case Report [PDF]

Iranian Journal of Neonatology, 2021
Background: Lumbosacral agenesis or caudal regression syndrome (CRS) is a rare congenital malformation represented with symmetrical sacrococcygeal or lumbosacrococcygeal agenesis with a varied incidence between 1 per 25000 live births to 2.5 per 100000 ...
Homa Babaei, Mina Khosravifar
doaj   +1 more source

Novel mutations expand the clinical spectrum of DYNC1H1-associated spinal muscular atrophy [PDF]

, 2015
OBJECTIVE To expand the clinical phenotype of autosomal dominant congenital spinal muscular atrophy with lower extremity predominance (SMA-LED) due to mutations in the dynein, cytoplasmic 1, heavy chain 1 (DYNC1H1) gene.
Al-Lozi, Muhammad T, Baas, Frank, Baloh, Robert H, Benatar, Michael, Calissano, Mattia, Chong, W K Kling, Cirak, Sebahattin, Connolly, Anne M, de Goede, Christian G E L, De Visser, Marianne, Fallon, Penny, Foley, A Reghan, Hadjikoumi, Irene, Hafezparast, Majid, Harms, Matthew B, Klein, Andrea, Mansour, Sahar, Manzur, Adnan Y, Martínez Arroyo, Amaia, Mcwilliam, Catherine, Mercuri, Eugenio, Muntoni, Francesco, Nixon, John, Overweg-Plandsoen, W C G Truus, Phadke, Rahul, Pitt, Matthew, Reilly, Mary M, Robb, Stephanie, Rodriguez Sanz, Aida, Rossor, Alexander M, Scoto, Mariacristina, Sewry, Caroline, Taylor, J Paul, Yang, Michele   +33 more
core   +1 more source