Results 81 to 90 of about 4,362 (269)

2D and 3D Classification Systems for Adolescent Idiopathic Scoliosis: Clinical Implications and Technological Advances

Orthopaedic Surgery, Volume 17, Issue 4, Page 999-1020, April 2025.
This study compares traditional 2D scoliosis classification systems (e.g., King, Lenke, and PUMC) with emerging 3D systems. It highlights the limitations of 2D methods and the advantages of integrating 3D models for more precise treatment planning and outcomes.
Wenqing Wei, Liang Cheng, Yating Dong, Tianyuan Zhang, Yaolong Deng, Jiale Gong, Fang Xie, Junlin Yang   +7 more
wiley   +1 more source

Treatment of clubfoot in young children with arthrogryposis by Ponseti method: possibilities and perspectives

Travmatologiâ i Ortopediâ Rossii, 2016
Background. Clubfoot is the most common deformity in arthrogryposis and is characterized by a high degree of rigidity and a tendency to relapse. At present, no consensus exists on the issue of treatment of this pathology.
D. V. Derevyanko, O. E. Agranovich, D. S. Buklaev, E. V. Petrova, S. I. Trofimova   +4 more
doaj   +1 more source

Use of a large gauge needle for percutaneous sectioning of the Achilles tendon in congenital clubfoot [PDF]

, 2010
OBJETIVO: Avaliar a técnica de secção percutânea do tendão calcâneo com a utilização de agulha de grosso calibre para correção do equino residual do pé torto congênito tratado pelo método de Ponseti. MÉTODO: Foram avaliadas prospectivamente 57 secções do
MARANHO, Daniel Augusto Carvalho, NOGUEIRA-BARBOSA, Marcello Henrique, SIMÃO, Marcelo Novelino, VOLPON, José Batista   +3 more
core   +2 more sources

Rapid Whole Genome Sequencing Uncovers a Triple Diagnosis: X‐Linked Chondrodysplasia Punctata, MECP2‐Related Disorder, and Mosaic Jacobs Syndrome

Molecular Genetics &Genomic Medicine, Volume 13, Issue 2, February 2025.
Neonate was found to have X‐linked chondrodysplasia punctata, MECP2‐related disorder, and mosaic Jacobs syndrome, highlighting the utility of advanced genetic testing in directing neonatal care and the complexity of managing multiple genetic diagnoses, while also adding to our understanding of the MECP2‐related disorder phenotypes in boys.
Megan Samuels, Kathleen Shields, Paul Hillman, Laura Farach   +3 more
wiley   +1 more source

Posteromedial Release versus Ponseti Treatment of Congenital Idiopathic Clubfoot: A Long-Term Retrospective Follow-Up Study into Adolescence

Therapeutics and Clinical Risk Management, 2020
Andrei Corbu,1,2 Dan Ionut Cosma,1,3 Dana Elena Vasilescu,3 Stefan Cristea2 1Department of Orthopedics and Traumatology, Clinical Rehabilitation Hospital Cluj-Napoca, Cluj, Romania; 2Department of Orthopedics and Traumatology, University of Medicine and ...
Corbu A, Cosma DI, Vasilescu DE, Cristea S   +3 more
doaj  

Ponseti Method versus surgical treatment in a teenage girl with neglected clubfoot: a case report

Foot & Ankle Surgery: Techniques, Reports & Cases, 2023
Introduction: Congenital clubfoot is the most common foot deformity. It affects 1 - 7/1000 live births. Clubfoot is considered neglected when it has not been treated before the child walks.
Camila Ordóñez-Reyes, Manuela Quiroga-Carrillo, María Fernanda García-Rueda, Martha Lorena Caicedo-Gutiérrez, Diego Fernando Ortiz Montoya, Jose A. Morcuende   +5 more
doaj   +1 more source

Early results of clubfoot management by ponseti method [PDF]

International Journal of Orthopaedics Sciences, 2017
Aim: Since long Clubfoot has been an unsolved clinical challenge for the orthopaedic surgeons. It is one of the commonest congenital deformities in children. More than 1,00,000 babies are born worldwide each year with congenital clubfoot. Around 80% of the cases occur in developing nations like India.
Dr. Kaustubh M Chauhan, Dr. Gaurav M Meda, Dr. Gaurang M Patel, Dr. Hemant H Mathur   +3 more
openaire   +1 more source

Patient with a heterozygous pathogenic variant in CSNK2A1 gene: A new case to update the Okur–Chung neurodevelopmental syndrome

American Journal of Medical Genetics Part A, Volume 194, Issue 9, September 2024.
Abstract The autosomal dominant Okur–Chung neurodevelopmental syndrome (OCNDS: OMIM #617062) is a rare neurodevelopmental disorder first described in 2016. Features include developmental delay (DD), intellectual disability (ID), behavioral problems, hypotonia, language deficits, congenital heart abnormalities, and non‐specific dysmorphic facial ...
Albin Blanc, Céline Bonnet, Marion Wandzel, Virginie Roth, Yannis Duffourd, Hanna Safraou, Bruno Leheup, Florence Muller, Julie D Colne, François Feillet, Emmanuelle Schmitt, Matheus Castro, Jullian Savatt, Adriano Burcheri, Christophe Nemos, Christophe Philippe, Laëtitia Lambert   +16 more
wiley   +1 more source

Investigating the association between vitamin D dietary intake during pregnancy and incidence of clubfoot in neonates

Birth Defects Research, Volume 116, Issue 1, January 2024.
Abstract Aims Talipes equinovarus (clubfoot) is a congenital lower foot deformity that results from a neuromuscular deficiency, but the precise etiology remains elusive. Vitamin D is important for fetal neuromuscular development. In this study, we investigated the association between dietary vitamin D intake during pregnancy and incidence of clubfoot ...
Haitham T. Idriss, Martha M. Werler
wiley   +1 more source

Factors Related to Early Recurrence of Idiopathic Clubfoot Post the Ponseti Method [PDF]

Malaysian Orthopaedic Journal, 2019
INTRODUCTION: Idiopathic clubfoot or congenital talipes equinovarus (CTEV) is managed by the Ponseti method worldwide; however, the recurrence of the deformity is a challenging problem.
Limpaphayom N, Sailohit P
doaj   +1 more source