Results 21 to 30 of about 1,395 (175)

Does laterality of deformity influence the severity of the idiopathic clubfoot?

open access: yesNigerian Journal of Medicine, 2019
BACKGROUND: The idiopathic clubfoot has been widely reported as the commonest congenital deformity of the lower limbs with incidence of approximately 1-2 in 1000 live births. Its exact aetiology is not known.
C O Anisi   +4 more
doaj   +1 more source

Descriptive epidemiology of idiopathic clubfoot [PDF]

open access: yesAmerican Journal of Medical Genetics Part A, 2013
AbstractClubfoot is a common structural malformation, occurring in approximately 1/1,000 live births. Previous studies of sociodemographic and pregnancy‐related risk factors have been inconsistent, with the exception of the strong male preponderance and association with primiparity.
Martha M, Werler   +7 more
openaire   +2 more sources

Reconstructive surgery in recurrent deformity (clubfoot relapse)

open access: yesГений oртопедии, 2021
Introduction Recurrent clubfoot deformity may be due to either an imperfect initial correction, or a natural history of a severe disease. In the later, idiopathic clubfoot is uncommon.
Pierre Lascombes   +2 more
doaj   +1 more source

Clubfeet and congenital constriction band syndrome

open access: yesEuropean Journal of Medical Research, 2021
Background Clubfeet and constriction band syndrome is a very rare non-idiopathic condition. Treatment is often difficult and the recurrence deformity rate is high.
Bujar Shabani, Dafina Bytyqi, Cen Bytyqi
doaj   +1 more source

Collaboration between Paediatrician and Orthopaedician in Management of Congenitial Talipes Equino Varus by Ponseti Method [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2020
Introduction: Congenital Talipes Equino Varus (CTEV) or Clubfoot is one of the commonest orthopaedic problems observed in infants. Deformity involving in utero malalignment of calcaneo-talar-navicular complex of the foot is known as CTEV. Due to lack
JB SANTHOSHA, SP AKSHATHA
doaj   +1 more source

Neurodevelopmental difficulties in children with idiopathic clubfoot [PDF]

open access: yesDevelopmental Medicine & Child Neurology, 2018
AimTo evaluate neurodevelopmental difficulties in children with idiopathic clubfoot.MethodA cross‐sectional study of 106 children (29 females, 77 males; aged 8–10y) with idiopathic clubfoot and 109 age‐, sex‐, and residential area‐parallelized children from the general population.
Elin Lööf   +4 more
openaire   +3 more sources

Gait in 5-year-old children with idiopathic clubfoot: A cohort study of 59 children, focusing on foot involvement and the contralateral foot

open access: yesActa Orthopaedica, 2016
Background and purpose — Idiopathic clubfoot can be bilateral or unilateral; however, most studies of gait have assessed clubfoot cases as one uniform group.
Elin Lööf   +4 more
doaj   +1 more source

NONSURGICAL TREATMENT OF CONGENITAL CLUBFOOT: RESULTS AND PERSPECTIVES

open access: yesTravmatologiâ i Ortopediâ Rossii, 2011
The results of 10 years of nonsurgical treatment of 350 children with idiopathic congenital clubfoot by different methods at the same hospital are compared.
I. Yu. Klychkova   +2 more
doaj   +1 more source

Challenging clubfeet: The arthrogrypotic clubfoot and the complex clubfoot

open access: yesJournal of Children's Orthopaedics, 2019
Within the realm of clubfoot deformities, teratologic and complex (or atypical) clubfeet stand out as the most difficult. Exemplarities of the teratologic types of clubfoot are those associated with arthrogryposis multiplex congenita.
H. J. P. van Bosse
doaj   +1 more source

Comparative Analysis between Podography and Radiography in the Management of Idiopathic Clubfeet by Ponseti Technique [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2017
Introduction: Idiopathic clubfoot is one of the most common and oldest congenital foot anomalies. There are controversies regarding its optimum management protocol and methodologies to be employed for its functional outcome evaluation.
VIKAS TRIVEDI   +2 more
doaj   +1 more source

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