Results 71 to 80 of about 1,992 (211)

Frequency of percutaneous achilles tenotomy in the treatment of idiopathic clubfoot using the ponseti method

open access: yesNigerian Journal of Medicine, 2018
Background: Percutaneous Achilles tenotomy is an integral component of congenital clubfoot treatment using the Ponseti method. This study was designed to assess the frequency and outcome of percutaneous Achilles tenotomy in the conservative treatment of ...
Chukwuemeka Okechukwu Anisi   +2 more
doaj   +1 more source

Routine 36‐week scan: diagnosis of fetal abnormalities

open access: yesUltrasound in Obstetrics &Gynecology, Volume 65, Issue 4, Page 427-435, April 2025.
ABSTRACT Objectives To investigate further the incidence and types of fetal abnormality identified at a routine 36‐week ultrasound examination, which had not been diagnosed in previous scans at 20 weeks and 12 weeks' gestation, and to report the fetal abnormalities that are diagnosed only postnatally.
A. Syngelaki   +5 more
wiley   +1 more source

Evaluation of an E-Learning Course for Clubfoot Treatment in Tanzania: A Multicenter Study

open access: yesJournal of Medical Education and Curricular Development, 2018
In total, 80% of clubfoot cases occur in low- and middle-income countries, where lack of clinical knowledge of the Ponseti method of treatment presents as a major barrier to treatment.
Silvia D Vaca   +5 more
doaj   +1 more source

Factors associated with the relapse in Ponseti treated congenital clubfoot

open access: yesBMC Musculoskeletal Disorders, 2022
Objectives We retrospectively investigated the clinical materials to seek the factors that lead to relapse after using the Ponseti method. Methods We retrospectively reviewed all children with congenital clubfoot treated with the Ponseti method in our ...
Wei Hu   +6 more
doaj   +1 more source

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

open access: yesOrthopaedic 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   +7 more
wiley   +1 more source

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

open access: yesMolecular 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   +3 more
wiley   +1 more source

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

open access: yesTherapeutics 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   +3 more
doaj  

Early results of clubfoot management by ponseti method [PDF]

open access: yesInternational 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   +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

open access: yesAmerican 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   +16 more
wiley   +1 more source

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

open access: yesTravmatologiâ 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   +4 more
doaj   +1 more source

Home - About - Disclaimer - Privacy