Results 61 to 70 of about 6,783 (160)

Variant Update on ASCC1 : Characterization of the First Homozygous Missense Variant Involved in Prenatal‐Onset Spinal Muscular Atrophy With Congenital Bone Fractures 2

American Journal of Medical Genetics Part A, Volume 200, Issue 3, Page 744-748, March 2026.
ABSTRACT Spinal muscular atrophy with congenital bone fractures 2 is a rare and severe autosomal recessive neuromuscular disorder caused by pathogenic variants in ASCC1. This condition characterized by prenatal onset of severe hypotonia with fetal hypokinesia and congenital contractures results in arthrogryposis multiplex congenita, and increased ...
A. Civit, L. Kerbellec, D. Laurenceau, D. C. Ung, M. P. Moizard, N. Ronce, P. Gueguen, F. Laumonnier, A. C. Bréhin, F. Marguet, A. Laquerrière, A. M. Bergemer Fouquet, J. Cirier, S. Blesson, S. Arpin, M. Jeanne, M. L. Vuillaume   +16 more
wiley   +1 more source

Current conservative management and classification of club foot: A review

Journal of Pediatric Rehabilitation Medicine, 2016
Clubfoot, known as congenital talipes equinovarus, is one of the complex paediatric foot deformity with the incidence of 1 in every 1000 live births. It consists of four complex foot abnormalities such as forefoot adductus, midfoot cavus, and hindfoot ...
Ganesan Balasankar, Ameersing Luximon, Adel Al-Jumaily   +2 more
doaj   +1 more source

Recurrent Constellations of Embryonic Malformations (RCEM): Teratogenicity Linked to Transient Hypoxia and Hormone Pregnancy Tests Agrees With RCEM and Suggest a Reactive Oxygen Species Pathogenesis

Birth Defects Research, Volume 118, Issue 3, March 2026.
ABSTRACT Background No consistent genetic etiology has been found for a group of six different conditions in humans with multiple malformations called “recurrent constellations of embryonic malformations” (RCEM). Recent studies indicate hypoxia/reoxygenation and generation Reactive Oxygen Species (ROS) as an underlying mechanism for RCEM with the ...
Aaron P. Adam, Helen E. Ritchie, Margaret P. Adam, Bengt R. Danielsson   +3 more
wiley   +1 more source

The clubfoot assessment protocol (CAP); description and reliability of a structured multi-level instrument for follow-up [PDF]

, 2005
Background In most clubfoot studies, the outcome instruments used are designed to evaluate classification or long-term cross-sectional results. Variables deal mainly with factors on body function/structure level.
Hanneke Andriesse, Gunnar Hägglund, Gun-Britt Jarnlo, H Bensahel, K Fukuhara, IV Ponseti, A Sirca, ML Zimny, GW Simon, D Atar, H Bensahel, A Catterall, E Cohen-Sobel, A Dimeglio, SJ Laaveg, S Pirani, DW Mc Kay, MG Uglow, AR Harvey, BD Roye, JM Flynn, AM Wainwright, World Health Organization, DG Altman, J Cohen, M Haas, HL Kundel, E Roos, NA Sgaglione, LH Daltroy, AC Plint, NL Young, A Campos da Paz, WJ Rejeski, JA Katula, MV Johnston, AJ Harrold, IV Ponseti   +37 more
core   +2 more sources

Risk factors associated with congenital clubfoot in children

Гений oртопедии
Introduction Congenital clubfoot is a frequent malformation of the lower extremities. However, the causes of this pathology in children are still unclear.
Maxim V. Vlasov, Irina V. Musikhina
doaj   +1 more source

Mid-term results of ponseti method for the treatment of congenital idiopathic clubfoot - (A study of 67 clubfeet with mean five year follow-up)

Journal of Orthopaedic Surgery and Research, 2011
Background Long-term success reports by Dr. Ponseti with the Ponseti method in the treatment of congenital idiopathic clubfoot have led to a renewed interest in this method among pediatric orthopedists.
Chavda Hiral R, Parmar Dipak S, Porecha Milind M   +2 more
doaj   +1 more source

What is a good result after clubfoot treatment? A Delphi-based consensus on success by regional clubfoot trainers from across Africa.

PLoS ONE, 2017
BackgroundCongenital talipes equino-varus (CTEV), also known as clubfoot, is one of the most common congenital musculoskeletal malformations. Despite this, considerable variation exists in the measurement of deformity correction and outcome evaluation ...
Tracey Smythe, Andrew Wainwright, Allen Foster, Christopher Lavy   +3 more
doaj   +1 more source

Knowledge and Attitude of Women in Reproductive Age toward Clubfoot in Cikeruh Village, Jatinangor Sub−district in 2014

Althea Medical Journal, 2018
Background: Clubfoot is a congenital anomaly which the ankle is twisted outward from the normal position. Clubfoot is the most common birth defect that can cause disability in the world.
F. M. Dicky Fitraendi, Fathurachman Fathurachman, Nugroho Harry Susanto   +2 more
doaj   +1 more source

Early versus late termination for fetal anomalies: Women's perspectives and psychological impact in a mixed methods study

Acta Obstetricia et Gynecologica Scandinavica, Volume 105, Issue 3, Page 444-454, March 2026.
This mixed method study evaluated the psychological impact and perspectives associated with early and late termination of pregnancy (TOP). Early TOP due to fetal anomalies is associated with a lower psychological impact compared to late TOP. Pregnancy termination has a substantial emotional impact regardless of gestational age.
Eline E. R. Lust, Kim Bronsgeest, Lidewij Henneman, Neeltje M. T. H. Crombag, Caterina M. Bilardo, Robert‐Jan H. Galjaard, Esther Sikkel, Audrey B. C. Coumans, Ayten Elvan‐Taşpınar, Sander Galjaard, Attie T. J. I. Go, Gwendolyn T. R. Manten, Eva Pajkrt, Elisabeth van Leeuwen, Monique C. Haak, Mireille N. Bekker   +15 more
wiley   +1 more source

A rare accessory muscle as a less recognized factor in clubfoot recurrence: A systematic review and three cases presentation

Foot & Ankle Surgery: Techniques, Reports & Cases
Congenital Talipes Equinovarus or Clubfoot is the most common congenital foot malformation in newborns, with recurrence rates of 14–40 % despite optimal treatment.
Lubenga Ali Baba Athos, MD, Shchukin Andriy, MD, Beyer Benoît, PhD, Ngomba Wa Ilunga Sylvie, MD, Nyembo Selemani Emile, MD, Arung Kalau Willy, PhD, MD, Panda Mulefu Jules, PhD, MD, Dereymaeker Greta, PhD, MD, Van Sint Jan Serge, PhD   +8 more
doaj   +1 more source