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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4631745 | PMC |
| http://dx.doi.org/10.5114/pwki.2015.54026 | DOI Listing |
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A narrow complex tachycardia with a short HV interval: What is the mechanism?
Pacing Clin Electrophysiol
January 2025
Division of Cardiology, the First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
The case was a 15-year-old male with a history of paroxysmal supraventricular tachycardia refractory to medical therapy and prior catheter. A repeat electrophysiology study and catheter ablation were applied. Baseline AH and HV intervals were 100 and 55 ms during normal sinus rhythm (NSR), respectively.
View Article and Find Full Text PDFIsolated Left Extensor Hallucis Longus Palsy Secondary to Deep Peroneal Nerve Injury in a 15-Year-Old Boy: A Case Report.
J Orthop Case Rep
November 2024
Department of Orthopaedic Surgery, The Johns Hopkins University School of Medicine, 1800 Orleans Street, Baltimore, MD 21287.
Introduction: Nerve palsies are potential consequences of fractures that can result in temporary loss of muscular function. Nerve palsies have not been extensively described in the context of tibial tubercle fractures in the pediatric population. Although the symptoms accompanying nerve palsies concern patients, evidence suggests that non-operative management often results in full functional recovery over time.
View Article and Find Full Text PDFPediatric Dent disease presenting with rickets and end-stage renal disease: case report and literature review.
J Int Med Res
September 2024
Department of Nephrology, Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Article Synopsis
- * A case report details a 15-year-old boy with a specific genetic mutation related to Dent disease who experienced joint pain (arthralgia) and bone softening (rickets) before being diagnosed with end-stage renal disease.
- * The case highlights that symptoms like joint pain and bone issues could indicate a rare underlying problem such as Dent disease, emphasizing the need for awareness and further investigation in similar cases.
A rare pediatric case of FDG-avid synovial herniation pits.
Radiol Case Rep
December 2024
Department of Nuclear Medicine and PET, The Prince of Wales and Sydney Children's Hospitals, Randwick, NSW 2031, Australia.
Synovial herniation pits are benign, round radiolucent lesions surrounded by a thin sclerotic rim within the superolateral aspect of the proximal femoral neck that are most commonly seen in the physically active adult population. Here we report, to the best of our knowledge, the first pediatric case of synovial herniation pits showing focal FDG uptake on a PET/CT scan in a 15 year old boy with Hodgkin's Lymphoma.
View Article and Find Full Text PDFBethlem myopathy: A novel homozygous variant of c.385C>T (p.Arg129Cys) in the COL6A2 gene.
Clin Case Rep
August 2024
Department of Medical Genetics, School of Medicine Iran University of Medical Sciences Tehran Iran.
Key Clinical Message: This case highlights the challenges in diagnosing Bethlem myopathy, the need for a high index of suspicion, and the importance of recognizing the diverse clinical presentations of this rare condition. Enhanced understanding can aid in early diagnosis and tailored management.
Abstract: Bethlem myopathy (BM), a rare collagen VI-related myopathy, is characterized by progressive muscle weakness and contractures, typically affecting the proximal muscles and joints.
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