Results 61 to 70 of about 263,235 (193)

A study on management of congenital clubfoot by Ponsetti technique in a rural medical college in India [PDF]

, 2018
Background: Congenital clubfoot also known as CTEV (congenital talipus equinovarus) is a common and debilitating congenital musculoskeletal anamoly affecting the children across the world with a slight preponderence in third world countries.
Jahan, Alamgir, Dar, Mohd Yahya, Jan, Wazir Fahad, Bangroo, Firdous Ahmad   +3 more
core   +1 more source

Pregnancy outcomes following exposure to galcanezumab: Analysis of cases from the galcanezumab clinical trials and postmarketing database

Headache: The Journal of Head and Face Pain, EarlyView.
Abstract Objective This study was conducted to describe pregnancy outcomes reported following maternal or paternal exposure to galcanezumab in clinical trials and postmarketing surveillance. Background Galcanezumab is a calcitonin gene‐related peptide‐inhibiting monoclonal antibody indicated for the preventive treatment of migraine.
Irene Boz, Jan Lewis Brandes, Christopher Robinson, Maria Fernanda Scantamburlo Fernandes, Sarah Lipsius, LaRonda Morford, Enemona Emmanuel Adaji, Anaclara Prada Jardim, Holland C. Detke   +8 more
wiley   +1 more source

Kinect-based 3D assessment for clubfoot deformity: An exploratory study

, 2020
Congenital talipes equinovarus is a musculoskeletal pediatric foot deformity, which is characterized by midfoot cavus, forefoot adductus, hindfoot varus and equinus (CAVE).
Joanne Yip, Luximon, A, Balasankar Ganesan, Ganesan, B, Al-Jumaily, A, Adel Al-Jumaily, Mohamed-Amine Choukou, Yip, J, Ameersing Luximon, Choukou, MA   +9 more
core   +1 more source

Comparison of two treatment methods of congenital clubfoot in the orthopaedists’ opinion [PDF]

, 2017
Introduction. Clubfoot is the second most common birth defect of the lower limb. In Europe (including Poland) it concerns about 1-2 in 1000 newborns. What is characteristic for a clubfoot, is change in the foot shape and its impairment with preserving ...
Misztal-Okońska, Patrycja, Piotr Książek, Piotr Okoński, Książek, Piotr, Okoński, Piotr, Goniewicz, Mariusz, Marek Okoński, Okoński, Marek, Mariusz Goniewicz, Patrycja Misztal-Okońska   +9 more
core   +1 more source

ETIOPATHOGENESIS OF CONGENITAL CLUBFOOT

, 2023
Congenital clubfoot is one of the most common congenital malformations, affecting 1-3 per 1000 live births and occurring twice as often in male fetuses. Although it is called congenital, it is not an embryonic malformation but is a developmental deformity that occurs in the second trimester of pregnancy.
Sandrosean Argentina Petru, Polișciuc Snejana Ruslan   +1 more
openaire   +2 more sources

Prenatal Diagnosis of Recurrent Fetal Intracranial Hemorrhage and a Maternally Inherited COL4A1 Variant of Uncertain Significance: A Case Report With Maternal Reverse Phenotyping

Clinical Case Reports, Volume 14, Issue 11, November 2026.
ABSTRACT A 33‐year‐old woman with two consecutive pregnancies affected by fetal left periventricular germinal matrix hemorrhage (Grade IV) and progressive ventriculomegaly underwent trio whole‐exome sequencing. A heterozygous COL4A1 c.4249G>C (p.Gly1417Arg) variant, classified as a variant of uncertain significance, was identified in the fetus of the ...
Wei Shi, Hongjing Xu, Caihong Pu, Yuanzhong Liang, Ting Zhao, Xueli Wang, Zhenxing Liu, Chunhua Zhang, Ting Li, Fengquan He   +9 more
wiley   +1 more source

Consensus Guidelines for Diagnosis and Management of Pyruvate Dehydrogenase Complex Deficiency

Journal of Inherited Metabolic Disease, Volume 49, Issue 6, November 2026.
ABSTRACT Primary pyruvate dehydrogenase complex deficiency (PDCD) comprises a group of monogenic disorders caused by pathogenic variants in genes encoding subunits of, or regulatory components affecting, the pyruvate dehydrogenase complex. The clinical phenotype spans a broad continuum, ranging from early onset congenital lactic acidosis to infantile ...
Nandaki Keshavan, Julia Neugebauer, Marcello Bellusci, Enrico Bertini, Garry Brown, Niklas Darin, Suzanne DeBrosse, Lucy Drexler, Stefan Drexler, Gregory M. Enns, Rebecca D. Ganetzky, Kelly Gilbert, Austin Larson, Rebecca Legi, April N. Lehman, Camile Newby, Manuel Schiff, Rachel Skeath, Peter W. Stacpoole, Sarah Thompson, Emma Watt, Saskia B. Wortmann, Jirair K. Bedoyan, Shamima Rahman   +23 more
wiley   +1 more source

Anatomical–Motor Level Discrepancy in Prenatal Diagnosis of Open Spinal Dysraphism: A 12‐Year Retrospective Observational Study

BJOG: An International Journal of Obstetrics &Gynaecology, Volume 133, Issue 12, Page 2188-2195, November 2026.
ABSTRACT Objectives To quantify the discrepancy between anatomical and motor levels in foetuses with open spinal dysraphism and identify prenatal factors associated with this difference. We also examined associations between anatomical level and ultrasound findings. Design Retrospective observational study.
Silvia Arévalo, Elena Moreno, Mar Meléndez, Carlos Giné, Carlota Rodó, Alba Casellas, Alba Farràs, Manel Mendoza, Nerea Maiz   +8 more
wiley   +1 more source

Two Novel ACTC1 Variants Cause Arthrogryposis Multiplex Congenita

Clinical Genetics, Volume 110, Issue 5, Page 584-589, November 2026.
We report on two individuals with arthrogryposis multiplex congenita who were heterozygous for ACTC1 missense variants (NM_005159.5; c.325G>A, p.Glu109Lys and c.650A>C, p.Lys217Thr) and provide a characterization of these variants through in vitro studies.
Lauren Kerr, Pierre Moffatt, Lauren Hyer, Sarah Nossov, Noémi Dahan‐Oliel, Frank Rauch   +5 more
wiley   +1 more source

THE ERRORS, COMPLICATIONS AND MEASURES FOR ITS PREVENTION IN THE TREATMENT OF SCHOOL AGE CHILDREN WITH CONGENITAL RECURRENT CLUBFOOT BY ILIZAROV METHOD

Travmatologiâ i Ortopediâ Rossii, 2012
Objective. To analyze the errors and complications of treatment of school age children with congenital recurrent clubfoot, treated in RISC «RTO» by transosseous osteosyntesis. Material and methods.
S. S. Leonchuk, G. P. Ivanov, A. S. Neretin, I. I. Martel, V. A. Shestakov   +4 more
doaj   +1 more source