Results 1 to 10 of about 4,149 (222)

An investigation of maternal psychological status of children with congenital talipes equinovarus treated with the Ponseti method [PDF]

Journal of Children's Orthopaedics, 2023
Objectives: To investigate maternal psychological status of children with congenital talipes equinovarus in different periods, and to clarify the influence on maternal psychological status of congenital talipes equinovarus treated with the Ponseti method.
Wentao Dong, Ningning Shi, Chunyu Wen, Yong Zhang   +3 more
doaj   +2 more sources

Management of Relapsed, Residual, and Resistant Idiopathic Congenital Talipes Equinovarus [PDF]

Journal of Orthopaedic Case Reports
Introduction: Congenital talipes equinovarus (CTEV) is a common pediatric deformity, with conservative management being the primary method of management.
Mohd Owais Ansari1, Yasir Salam Siddiqui1, Faisal Harun1, Tyson Rana1, Kaustubh Hari1, Mazhar Abbas1   +5 more
doaj   +2 more sources

Congenital talipes equinovarus: A literature review. [PDF]

Ann Med Surg (Lond), 2022
Congenital talipes equinovarus (CTEV) is a congenital disability characterized by leg deformities in the cavus, adducts, varus, and equinus. The etiology of CTEV is poorly understood, despite its incidence ranging from 0.76 to 3.49 cases per 1000 live births in Indonesia.
Mustari MN, Faruk M, Bausat A, Fikry A.
europepmc   +3 more sources

Does idiopathic congenital talipes equinovarus have an impact on attainment of developmental milestones? A multicentre international study. [PDF]

J Child Orthop, 2019
Purpose: The Ponseti method is a well-established approach to treating clubfoot. Potentially, both the underlying pathology and adherence to post-correction bracing can affect lower limb function and age of independent standing and walking.
Hughes K, Gelfer Y, Cokljat M, Wientroub S, Yavor A, Hemo Y, Dunkley M, Eastwood DM.   +7 more
europepmc   +3 more sources

An Observational Study on Pre-natal Diagnosis of Congenital Talipes Equinovarus [PDF]

Journal of Orthopaedic Case Reports
Introduction: Congenital talipes equinovarus (CTEV), or clubfoot, is a common congenital lower limb disorder. Pre-natal diagnosis using ultrasound (US) enables early identification, facilitating timely intervention and improving outcomes.
Gaurav Vatsa, Saurabh Suman, Siddharth Kumar Singh   +2 more
doaj   +2 more sources

Interventions for congenital talipes equinovarus (clubfoot). [PDF]

Cochrane Database Syst Rev, 2020
Congenital talipes equinovarus (CTEV), also known as clubfoot, is a common congenital orthopaedic condition characterised by an excessively turned-in foot (equinovarus) and high medial longitudinal arch (cavus). If left untreated it can result in long-term disability, deformity and pain.
Bina S, Pacey V, Barnes EH, Burns J, Gray K.   +4 more
europepmc   +6 more sources

The etiology of idiopathic congenital talipes equinovarus: a systematic review [PDF]

Journal of Orthopaedic Surgery and Research, 2018
Background Also known as clubfoot, idiopathic congenital talipes equinovarus (ICTEV) is the most common pediatric deformity and occurs in 1 in every 1000 live births.
Vito Pavone, Emanuele Chisari, Andrea Vescio, Ludovico Lucenti, Giuseppe Sessa, Gianluca Testa   +5 more
doaj   +2 more sources

A New Case of PITX1-Related Mandibular–Pelvic–Patellar (MPP) Syndrome [PDF]

Clinics and Practice
Background: The PITX1 gene encodes a transcription factor that plays a crucial role in the development of the lower limbs, pelvis, and structures derived from the first branchial arch.
Evgeniya Melnik, Ekaterina Petrova, Tatiana Markova, Ksenya Zabudskaya, Elena Dadali   +4 more
doaj   +2 more sources

Pie zambo sindrómico más allá de la artrogriposis y el mielomeningocele: tratamiento ortopédico con el método de Ponseti

Revista Española de Cirugía Ortopédica y Traumatología, 2021
Resumen: Introducción: El pie zambo supone una de las malformaciones congénitas del pie más frecuentes. Generalmente la etiología es idiopática.
E. Ferrando Meseguer, S. Roig Sánchez, L. Pino Almero, A. Romano Bataller, M.F. Mínguez Rey   +4 more
doaj   +1 more source

Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy. [PDF]

, 2020
Developmental and epileptic encephalopathies are a heterogeneous group of early-onset epilepsy syndromes dramatically impairing neurodevelopment. Modern genomic technologies have revealed a number of monogenic origins and opened the door to therapeutic ...
Alix, E, Alkaya, DU, Ashrafzadeh, F, Becker, F, Bilguvar, K, Chatron, N, de Bellescize, J, EuroEpinomics-RES consortium AR working group, Gunes, N, Hardies, K, Hussien, H, Karimiani, EG, Kok, F, Labalme, A, Lerche, H, Lesca, G, Maroofian, R, May, P, Morsy, H, Moslemi, A-R, Nabil, A, Najafi, M, Omar, T, Poulat, A-L, Ramos, L, Roselli, S, Sanlaville, D, Schmidts, M, Tajsharghi, H, Tuysuz, B, Weckhuysen, S   +30 more
core   +2 more sources