Results 51 to 60 of about 517,696 (136)

Investigating the Relationship Between Sensory Processing, Pain and Toe Walking Gait: A Survey Study

open access: yesJournal of Paediatrics and Child Health, EarlyView.
ABSTRACT Aim This study aimed to examine sensory processing patterns, the frequency and impact of parent‐reported pain in children who toe walk across a range of diagnoses using validated caregiver‐report tools. Methods An online cross‐sectional survey was distributed internationally between July 2024 and March 2025.
Jack H. Donne   +5 more
wiley   +1 more source

Moth‐Eaten Osteolysis of Multiple Foot Bones After a Conservatively Treated “Stable” Ankle Fracture: A Case Report and Literature Review

open access: yesClinical Case Reports, Volume 14, Issue 9, September 2026.
ABSTRACT Progressive multifocal “moth‐eaten” osteolysis involving foot and ankle bones after nonoperative treatment of a stable ankle fracture is rare and warrants evaluation for infectious, neoplastic, inflammatory, vascular, and mechanical causes.
Haotian Wu   +4 more
wiley   +1 more source

Predictive simulations identify potential neuromuscular contributors to idiopathic toe walking [PDF]

open access: yes
Background: Most cases of toe walking in children are idiopathic. We used pathology-specific neuromusculoskeletal predictive simulations to identify potential underlying neural and muscular mechanisms contributing to idiopathic toe walking.
Buizer, Annemieke I.   +20 more
core   +1 more source

Idiopathic toe walking: What’s New? An Integrative Review

open access: yesJournal of the Foot & Ankle
Objective: Consolidate the current knowledge on idiopathic toe walking, provide a critical overview, and identify areas for potential future research. Methods: An electronic search was conducted in the following databases up to June 2023: MEDLINE, EBSCO,
Letícia D’Ordaz Lhano Santos   +4 more
doaj   +1 more source

Gait Alterations Due to DCC Gene Variants in Individuals with Congenital Mirror Movements

open access: yesMovement Disorders Clinical Practice, Volume 13, Issue 9, Page 2154-2165, September 2026.
Abstract Background Congenital Mirror Movement Syndrome (CMMS) involves involuntary movements on one side of the body while voluntary movements are performed on the other side. They disrupt left–right coordination and can be caused by a pathogenic variant in the DCC gene.
Nok‐Yeung Law   +7 more
wiley   +1 more source

An introduction to the role of physical therapy in idiopathic toe walking [PDF]

open access: yes, 2011
Idiopathic toe walking (ITW) is a condition, whose cause is unknown, and characterized by a persistent tiptoe gait pattern without evidence of neurologic, orthopedic, or psychiatric disease.
Collins, Patrice
core   +1 more source

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

open access: yesJournal 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   +4 more
doaj   +1 more source

The Erasmus—Polyneuropathy Symptom Score for the Screening of Chronic Axonal Polyneuropathy: A Validation Study

open access: yesJournal of the Peripheral Nervous System, Volume 31, Issue 3, September 2026.
ABSTRACT Background and Aims Chronic axonal polyneuropathy is a common disorder that often remains undiagnosed. Early detection may enhance treatment of underlying risk factors and prevent long‐term complications. The Erasmus‐Polyneuropathy symptom score (E‐PSS) is a simple and rapid screening tool, consisting of six questions (score ranges 0–14). This
Noor E. Taams   +9 more
wiley   +1 more source

Genetic Factors Associated with Toe Walking in Children

open access: yesВопросы 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   +4 more
doaj   +1 more source

MDSGene Systematic Review of Common Forms of Dominant Hereditary Spastic Paraplegia: Novel Insights

open access: yesMovement Disorders Clinical Practice, Volume 13, Issue 8, Page 1804-1814, August 2026.
Abstract Background Hereditary spastic paraplegia (HSP) is a neurodegenerative disorder characterized by progressive spasticity and lower limb weakness. The most common forms of autosomal dominant HSP are caused by pathogenic variants in SPAST (SPG4 or HSP‐SPAST), ATL1 (SPG3A or HSP‐ATL1), and REEP1 (SPG31 or HSP‐REEP1).
Ce Kang   +24 more
wiley   +1 more source

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