Results 51 to 60 of about 11,582,569 (201)

Clubfoot and Osteogenesis imperfecta — A rare combination - Case report and review of the literature

Journal of Orthopaedic Reports, 2022
Background: The combination of Osteogenesis imperfecta (OI) and congenital talipes equinovarus (CTEV), or clubfoot is a very rare one. The associated bone fragility with OI makes it difficult for manipulation and casting.
Shubham Srivastava, Suresh Chand, Ajai Singh   +2 more
doaj   +1 more source

Ponseti method in the management of clubfoot under 2 years of age: A systematic review.

PLoS ONE, 2017
BackgroundCongenital talipes equinovarus (CTEV), also known as clubfoot, is common congenital orthopedic foot deformity in children characterized by four components of foot deformities: hindfoot equinus, hindfoot varus, midfoot cavus, and forefoot ...
Balasankar Ganesan, Ameersing Luximon, Adel Al-Jumaily, Suchita Kothe Balasankar, Ganesh R Naik   +4 more
doaj   +1 more source

Experience with accelerated ponseti technique for treatment of idiopathic clubfoot in a regional orthopaedic hospital in Nigeria

African Journal of Paediatric Surgery, 2023
Introduction: Idiopathic talipes equinovarus (ITEV) 'aka clubfoot' is the most common foot deformity in children. Ponseti technique had been accepted as a standard method for correction.
Omolade Ayoola Lasebikan, Wilson Ikpemhi Anetekhai, Joseph Effiong Asuquo, Ifeanyi Azubuike Anikwe, Gerald Chukwuemeka Oguzie, Innocent Egbeji Abang, Njoku Isaac Omoke, Best Joseph Asuquo   +7 more
doaj   +1 more source

Summary of variations in the Ponseti method and complications.

, 2018
Summary of variations in the Ponseti method and complications.
Gabriel Ferraz Ferreira (5993237), Kelly Cristina Stéfani (5993240), Davi de Podestá Haje (5993243), Monica Paschoal Nogueira (5888018)   +3 more
core   +1 more source

Outcomes of the Clubfoot Treatment with the Ponseti Method: Recurrence and Prognostic Factors

Journal of Orthopedic and Spine Trauma, 2022
Background: Clubfoot is a multifactorial disease with the prevalence of one in 1000 live births. The presentations of clubfoot are forefoot adductus, hindfoot varus, cavus, and equinus.
Arash Maleki, Seyed Reza Aghapour, Abaalfadel abbas saleh   +2 more
doaj   +1 more source

Relationship of Talar Dome Changes with Ankle Mobility in Conservatively Treated Idiopathic Congenital Equino-Varus Foot [PDF]

Malaysian Orthopaedic Journal
Introduction: The Ponseti technique (PT) is widely used for managing idiopathic congenital talipes equinovarus (CTEV), but it can lead to talar dome distortion and reduced ankle range of motion (ROM), resulting in compromise functional outcomes.
Chattopadhyay A, Sinha S, Raghav L, Gupta S, Sud A, Kanojia RK   +5 more
doaj   +1 more source

Congenital idiopathic atypical clubfoot [PDF]

The Egyptian Orthopaedic Journal, 2020
BackgroundThe Ponseti method has shown remarkable success in treating congenital idiopathic clubfoot. However, some feet with complex or atypical presentation do not respond to the standard protocol of manipulation and casting.Patients and methodsA total
Mohamed Osman
doaj   +1 more source

Clinical and radiological assessment before and after treatment using the Ponseti method.

, 2018
Clinical and radiological assessment before and after treatment using the Ponseti method.
Gabriel Ferraz Ferreira (5993237), Kelly Cristina Stéfani (5993240), Davi de Podestá Haje (5993243), Monica Paschoal Nogueira (5888018)   +3 more
core   +1 more source

Comparative study of accelerated ponseti method versus standard ponseti method for the treatment of idiopathic clubfoot

Journal of Orthopedics, Traumatology and Rehabilitation, 2018
Introduction: Clubfoot is a common congenital deformity with incidence of one in thousand live births. Ponseti method is currently the gold standard for treatment of clubfoot which conventionally involves weekly plaster changes. A prospective comparative study was carried out at our institute where we compared one group with weekly plaster change to ...
Mahendra Solanki, Anand Ajmera, Sanjay Rawat   +2 more
openaire   +2 more sources

Two Novel ACTC1 Variants Cause Arthrogryposis Multiplex Congenita

Clinical Genetics, Volume 110, Issue 5, Page 584-589, November 2026.
We report on two individuals with arthrogryposis multiplex congenita who were heterozygous for ACTC1 missense variants (NM_005159.5; c.325G>A, p.Glu109Lys and c.650A>C, p.Lys217Thr) and provide a characterization of these variants through in vitro studies.
Lauren Kerr, Pierre Moffatt, Lauren Hyer, Sarah Nossov, Noémi Dahan‐Oliel, Frank Rauch   +5 more
wiley   +1 more source