Results 61 to 70 of about 12,321 (201)

Idiopathic Toe Walking Treatment Methods

, 2023
Children’s walking and gait mechanics are ever changing as they are growing. Toe walking behavior is considered normal until the age of two. If there is no underlying condition contributing to the toe walking pattern, it’s considered idiopathic in nature.
Perry, Eva
core  

Idiopathic Toe Walking: An Update on Natural History, Diagnosis, and Treatment

Journal of the American Academy of Orthopaedic Surgeons, 2022
Toe walking is a common presenting report to an orthopaedic practice. Evaluation of a child with toe walking includes a thorough history and physical examination to elucidate the diagnosis.
J. Bauer, S. Sienko, J. Davids
semanticscholar   +1 more source

Tackling Anxiety‐ and Stress‐Related Freezing of Gait in People With Parkinson's Disease (TACKLING‐FOG): Study Protocol for a Randomized Controlled Trial

European Journal of Neuroscience, Volume 63, Issue 12, June 2026.
Participants undergo baseline assessment followed by randomization to either the intervention or a waitlist control condition. The intervention group receives four sessions immediately, while the waitlist group enters a 4‐week waiting period. Post‐intervention assessment is conducted in both groups, after which the waitlist group crosses over to ...
Gijs Vissers, Anouk Tosserams, Annelien A. Duits, Anouk van der Heide, Bastiaan R. Bloem, Rick C. Helmich, William R. Young, Jorik Nonnekes   +7 more
wiley   +1 more source

Efektivitas orthoses terhadap gait pattern pada anak idiopathic toe walking : study narrative review [PDF]

, 2022
Latar Belakang: : Ideopatic toe walking merupakan kondisi dimana terjadi kelainan pola berjalan ( hilangnya fase heel strike saat berjalan ). Untuk penyebabnya masih belum di ketahui namun ada beberapa factor resiko yang harus diperhatikan : gender ...
Siti Khotimah, SST.FT., M. Fis, Adinda Farida Larasati, 1810301183, Rizky Wulandari, SST, M.Fis   +2 more
core  

Adherence to serial casting protocols for idiopathic toe walking: A quality improvement initiative

Journal of Pediatric Rehabilitation Medicine, 2022
PURPOSE: This initiative aimed to assess adherence to Scottish Rite for Children’s serial casting protocol for children with idiopathic toe walking (ITW), factors related to adherence, and outcomes after education regarding the protocol.
Karina A. Zapata, Megan E. Trevino, Fabiola I. Reyes, Chan-Hee Jo, Charu Sharma   +4 more
doaj   +1 more source

A Difficult‐to‐Manage Case of Primary Idiopathic Erythromelalgia—Case Report

Clinical Case Reports, Volume 14, Issue 4, April 2026.
ABSTRACT Erythromelalgia is a rare condition with symptoms of erythema, warmth, and painful extremities exacerbated by warmth and relieved by cooling. Pain management is often challenging. The sodium channel blocker, lacosamide, was most effective in this patient.
Sarah Wide, Rajish S. K. Shil, Bernhard Frank, Viraj Bharambe   +3 more
wiley   +1 more source

Genetic Factors Associated with Toe Walking in Children

Вопросы современной педиатрии, 2020
The article describes genetic factors associated with toe walking in children. Association of gait abnormality with variants in genes listed below is shown: PMP22 (peripheral myelin protein 22), EGR2 (early growth response protein 2), AIFM1 (apoptosis ...
David Pomarino, Anneke Thren, Stefaine Morigeau, Johanna R. Thren, Anna A. Emelina   +4 more
doaj   +1 more source

Idiopathic toe-walking in childhood

Russian Journal of Child Neurology, 2020
Background. Idiopathic toe walking (ITW) in childhood is a benign age-dependent disorder of the normal walking formula.Objective: neurological, catamnestic and electromyographic analysis of patients with ITW.Materials and methods. The study group consisted of 59 patients aged 1 year 4 months to 15 years (mean age is 6.10 ± 3.54 years) with a ...
openaire   +3 more sources

Pycnodysostosis With Papilledema and Isolated Low Parathyroid Hormone Levels in an Eight‐Year‐Old Girl: A Genetically Confirmed Case Report

Clinical Case Reports, Volume 14, Issue 4, April 2026.
ABSTRACT Pycnodysostosis is a rare autosomal recessive skeletal dysplasia resulting from pathogenic variants in the CTSK gene, which encodes cathepsin K, a lysosomal cysteine protease expressed in osteoclasts. Deficiency of this enzyme leads to defective bone resorption and generalized osteosclerosis.
Meghana Krishna Kesineni, Naveen Jagadish Kandregula, Sameer Kumar Majety, Yulia Alekseevna Pimenova, Bhargav Kadali, Vineeth Potluri, Prudhvi Lekkala   +6 more
wiley   +1 more source

The Interplay Between IL‐6, Hepcidin, and BMPR2 Signalling in Pulmonary Arterial Hypertension: Mechanistic Insights Into Vascular Remodelling

Pulmonary Circulation, Volume 16, Issue 2, June 2026.
ABSTRACT Pulmonary arterial hypertension (PAH) is characterized by excessive pulmonary vasoconstriction and vascular remodelling, with mutations in bone morphogenetic protein receptor type 2 (BMPR2) being the most common genetic alteration associated with the disease.
Quezia K. Toe, Theo Issitt, Gregory J. Quinlan, S. John Wort   +3 more
wiley   +1 more source