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Approach to Case of Ataxia in Children
Ataxia in children is a neurological disorder characterized by impaired coordination, balance, and voluntary muscle movements. Ataxia is a term used to describe a group of disorders that affect the cerebellum, a part of the brain responsible for coordination and balance. There are various types of ataxia in children, including hereditary ataxias (genetic), acquired ataxias (due to injury or illness), and idiopathic ataxia (of unknown cause). Common symptoms include unsteady gait, tremors, difficulty with fine motor skills, slurred speech, and problems with eye movements. Hereditary ataxias often result from genetic mutations, while acquired ataxias may be caused by brain injuries, infections, or toxins. Diagnosis involves a thorough medical history, physical examination, neurological tests, and imaging studies like MRI or CT scans to assess the brain's condition. Management depends on the underlying cause. Symptomatic treatment may include physical and occupational therapy to improve motor skills and assistive devices for mobility. In cases of hereditary ataxia, genetic counseling is essential to assess the risk of passing on the condition to future generations. The prognosis varies based on the type and severity of ataxia. Some forms may be progressive, while others remain stable or improve with therapy.
About the Speaker
Kushal Dilip Ugale
Consultant Clinical Psychologist at Sunshine Counselling and Therapy Center
Dr. Anuradha Sanadhya is a highly respected professor of pediatrics at RNT Medical College in Udaipur. Her remarkable contributions extend beyond academia, as she has held leadership roles such as President and Secretary in various prestigious medical associations, including the IAP Udaipur branch and the Women's Wing of the Rajasthan State IAP.
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H. pylori Treatment with PYELRA®: Best Practices
PYLERA® is a medication used for the treatment of Helicobacter pylori (H. pylori) infection, a common cause of stomach ulcers and gastritis. It contains a combination of three active ingredients: bismuth subcitrate potassium, metronidazole, and tetracycline. This combination works synergistically to eradicate H. pylori bacteria and reduce associated symptoms. Treatment with PYLERA® typically involves taking multiple capsules four times a day for a specified duration, as prescribed by a healthcare provider. It is important to follow the treatment regimen as directed and to discuss potential side effects
Fluid Management and Hemodynamic Optimization
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Management of Pulmonary Fibrosis
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Ulcerative colitis: Diagnosis & Management
Ulcerative colitis is diagnosed through a combination of clinical evaluation, laboratory tests, imaging studies, and endoscopic examination of the colon. Key diagnostic tests include stool studies to rule out infections, blood tests for inflammatory markers like C-reactive protein and fecal calprotectin, and colonoscopy with biopsy to visualize the colon and confirm the diagnosis. Imaging studies like CT scans or MRI may be used to assess disease severity and complications such as toxic megacolon or perforation. Management of ulcerative colitis involves a step-wise approach, starting with anti-inflammatory medications like aminosalicylates for mild to moderate disease.Immunosuppressants such as corticosteroids, thiopurines, or biologics (e.g., anti-TNF agents) are used for moderate to severe disease or if patients do not respond to first-line therapy. Regular monitoring of disease activity through symptom assessment, blood tests, and endoscopic evaluation is crucial for disease management and to prevent complications.
Micronutrient Deficiencies
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