Results 51 to 60 of about 262,831 (164)

Impact of physiotherapy on the treatment of congenital muscular torticollis in 2-4 months infants. [PDF]

open access: yes, 2007
Subject of research: resolving of torticollis features in infants under the influence of physiotherapy. Problem of research: Congenital muscular torticollis is the most common form of torticollis in children.
Banionienė, Džiuljeta,
core   +1 more source

Uncovering the Genetic Landscape of Pediatric Hearing Loss Along the Texas–Mexico Border

open access: yesClinical Genetics, Volume 110, Issue 5, Page 627-636, November 2026.
Project GIVE provided evaluations and genome sequencing to 23 children with hearing loss along the Texas–Mexico border. Seventy percent received a molecular diagnosis and 56% of those diagnosed had changes to medical management. In this region, underdiagnosis of genetic hearing loss is due to care barriers rather than lower genetic burden.
Desiree Lanehart   +17 more
wiley   +1 more source

Planning a Clinical Practice Guideline Revision for a Core Set of Outcome Measures in Adults Undergoing Neurologic Physical Therapy, Part 2: Determining Stakeholders' Uptake and Recommendations

open access: yesClinical and Public Health Guidelines, Volume 3, Issue 4, October 2026.
ABSTRACT Objective To determine the uptake and recommendations for revision of the 2018 Clinical Practice Guideline (CPG): Core Set Outcome Measures for Adults with Neurologic Conditions Undergoing Rehabilitation. Design Online Survey. Setting Online with participants from multiple settings.
Jane E. Sullivan   +6 more
wiley   +1 more source

Effect of massage therapy on infants with congenital muscular torticollis: A retrospective comparative study

open access: yesFrontiers in Pediatrics, 2023
ObjectiveTo detect the effect and safety of massage therapy on infants with congenital muscular torticollis.MethodsA total of 56 infants with unilateral congenital muscular torticollis were enrolled in this retrospective comparative study.
Wei Tang   +9 more
doaj   +1 more source

Congenital Muscular Torticollis: A Case Report

open access: yesPhilippine Journal of Otolaryngology Head and Neck Surgery, 2019
Objective: To discuss a case of congenital muscular torticollis and its presentation, pathophysiology and management.  Methods:                     Design: Case Report                     Setting: Tertiary Private Hospital                    
Leila Marie Villanueva
doaj  

Congenital Muscular Torticollis: A current Concept Review

open access: yesSurgiColl
Torticollis is often characterized by a unilateral head tilt and rotation of the chin to the opposite side. This pathology is believed to arise from contracted, shortened, or deformed sternocleidomastoid muscle.
Pratik Pradhan   +4 more
doaj   +1 more source

A Novel De Novo MTM1 Insertion Frameshift Variant Causes X‐Linked Myotubular Myopathy in a Chinese Female

open access: yesMolecular Genetics &Genomic Medicine, Volume 14, Issue 10, October 2026.
A 24‐year‐old heterozygous woman presented with lifelong hypotonia and slowly progressive, asymmetric axial and limb‐girdle weakness with facial/ocular involvement and restrictive ventilatory impairment (FVC 53.12% predicted). Multimodal evaluation (EMG, muscle MRI, and whole‐exome sequencing [WES]) identified a de novo MTM1 frameshift variant ...
Lijun Chen, Yingxiao Bao, Gonglu Liu
wiley   +1 more source

Acute torticollis – Unusual presentation of acute disseminated encephalomyelitis

open access: yesCurrent Medicine Research and Practice
‘Torticollis’, or ‘head tilt’, is a term used to describe a twisted or turned neck. Torticollis can be categorised as either congenital or acquired. Acquired torticollis is frequently a symptom of underlying central nervous system (CNS) pathology.
Divya Agrawal   +3 more
doaj   +1 more source

A Case of Primary Intramedullary Infantile Fibrosarcoma With an RBPMS::NTRK3 Fusion and Response to Larotrectinib

open access: yesNeuropathology and Applied Neurobiology, Volume 52, Issue 5, October 2026.
We report a case of primary intramedullary infantile fibrosarcoma (IFS) in a 4‐week‐old infant with rapidly progressive cervical myelopathy. Histology showed a spindle cell tumour with diffuse S100 and pan‐TRK expression. RNA sequencing identified an RBPMS::NTRK3 fusion.
Mégane Le Quang   +8 more
wiley   +1 more source

Infantile-Onset LMNA-Related Congenital Muscular Dystrophy Presenting as Torticollis: A Case Report

open access: yes, 2023
Lamin A (LMNA)-related congenital muscular dystrophy usually presents with hypotonia and severe axial muscle weakness in early infancy. We report a patient who initially presented with torticollis but was finally diagnosed with LMNA-related congenital ...
Ji Ae Kim   +4 more
core   +1 more source

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