Results 81 to 90 of about 11,582,569 (201)
Background Little information was obtained from the published papers about the kinematic coupling effect between tarsal bones during Ponseti manipulation. The aim was to explore the kinematic coupling effect of the joints around talus, to investigate the
Song-Jian Li +3 more
doaj +1 more source
Congenital Clubfoot Treated with the Ponseti Method
Purpose: This study examined the Ponseti method for the nonsurgical treatment of a congenital clubfoot. Materials and Methods: A total of 35 patients (52 clubfeet) were evaluated. All patients were treated by serial manipulation and casting as described by Ponseti.
Jong Sup Shim +3 more
openaire +1 more source
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
Purpose The aim of the study was to examine motor abilities in children treated for idiopathic clubfoot with either the traditional extensive surgery method or the Ponseti method, and compare their motor skills with a control group without clubfoot ...
V. S. Aulie, V. B. Halvorsen, J. I. Brox
doaj +1 more source
MANAGEMENT OF ATYPICAL CLUBFOOT BY PONSETI METHOD
From May 2006 to August 2009 analyzed 28 clinical observations (34 feet) for children aged from 7 days to 1.5 years with severe atypical congenital clubfoot (Pirani 5,6 points), treated by the method of I. Ponseti. The average number of gypsum one foot to the full correction was - 6.3. It was written 38 achillotomy.
V. F. Blandinsky +3 more
openaire +3 more sources
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
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
Congenital talipes equinovarus (CTEV), also known as clubfoot, is a complex congenital deformity of the foot that, left untreated, can limit a person’s mobility by making it difficult and painful to walk. Worldwide, 80% of children born with clubfoot are
Rohit Malhotra +5 more
doaj +1 more source
Overcoming Barriers: A Study on Family Experiences and Treatment Adherence in Congenital Talipes Equinovarus in Kutch District, Gujarat [PDF]
Background: The Ponseti method is widely recognized as the gold standard for managing congenital clubfoot, offering an effective, low-cost alternative to surgical interventions.
Vishal Pushkarna +2 more
doaj +1 more source
Factors associated with the relapse in Ponseti treated congenital clubfoot
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

