Myositis diagnosis in hindi

हाल ही में अभिनेत्री सामंथा रुथ प्रभु ने सोशल मीडिया पर जाहिर किया है कि वह मायोसाइटिस नामक एक ऑटोइम्यून कंडीशन की शिकार हो गई हैं। इसके बाद से ही उनके प्रशंसक अभिनेत्री के स्वस्थ होने की दुआएं कर रहे हैं साथ ही इस बीमारी के बारे में सर्च भी करने लगे हैं। दरअसल इस बीमारी में मसल्‍स कमजोर होने लगती हैं। आइए जानते हैं इस बीमारी के बारे में... दवाएं - विभिन्न प्रकार की दवाएं मायोसाइटिस का कारण बन सकती हैं। सबसे आम दवा प्रकारों में से एक जो मायोसाइटिस का कारण बन सकता है वह स्टैटिन है। स्टैटिन ऐसी दवा है जिनका उपयोग हाई कोलेस्ट्रॉल को कम करने में किया जाता है। स्टैटिन थेरेपी का सबसे आम साइड इफेक्‍ट मसल्‍स में दर्द है। लेकिन स्टेटिन थेरेपी से मायोसाइटिस होने की संभावना कम है।

Actor Samantha Ruth Prabhu has recently opened up about being diagnosed with an autoimmune condition called myositis. She shared a post on Instagram in which she wrote, "This too shall pass." Myositis is a condition in which the patient experiences inflammation in the muscles. It is an autoimmune condition which can also be a result of some infection, injury or drug side effect. According to National Health Service UK (NHS), myositis is the name for a group of rare conditions which lead to weak, painful and aching muscles. Also, this condition gets worse with time. There are generally three types of myositis: Polymyositis, dermatomyositis and inclusion body myositis (IBM). What are the symptoms of myositis? Muscle weakness is the main symptom of myositis. While some patients may experience muscle pain, others may not. Other symptoms of this condition include aching muscles, constant tiredness, difficulty in sitting, discomfort in swallowing and depression. It may also become hard to complete daily tasks like climbing stairs, combing hair, lifting objects and more. What are the causes of myositis? According to NHS, myositis is caused by some problem in one's immune system due to which it mistakenly attacks the healthy tissues. However, there are different possible causes of myositis. Many cases do not have a cause. At the same time, others are a result of an injury or infection. A few researchers have also found that drug toxicity, viruses such as common cold, flu or HIV or...

Diagnosing any disease is a bit like solving a mystery. The physician will collect a variety of information and fit this all together to form an understanding about what is causing the patient’s symptoms. For those with myositis, this process can be challenging for a number of reasons. • Myositis diseases are rare, which means that clinicians may not be immediately aware of what to look for. • Myositis often starts out looking like a number of different autoimmune diseases. • Myositis takes a number of different forms, each of which is also very diverse. • Myositis can occur in combination with other overlapping autoimmune diseases. • Myositis symptoms are different in every patient. The first step in any diagnosis is a medical history. The doctor will ask questions about your health in general, including detailed personal and family health histories. Then he or she will want to know about your symptoms: when you first saw signs of the skin rash, what made you first notice muscle weakness, whether you did anything to treat these symptoms yourself, whether there are certain things (foods, activities, weather) that make the symptoms better or worse, whether you had an infection or other illness around the time the symptoms started. The next step will be a physical examination. The doctor will examine your skin symptoms and test your muscle strength. He or she may ask you to demonstrate activities that are difficult because of the weakness, such as walking up steps, lifting y...

Autoimmune myositis is characterized by inflammatory and degenerative changes in the muscles (polymyositis, necrotizing immune-mediated myopathy) or in the skin and muscles (dermatomyositis). Manifestations include symmetric weakness, occasionally tenderness, and fibrous replacement of muscle, sometimes with atrophy, principally of the proximal limb girdle muscles. Diagnosis is by clinical findings and abnormalities on muscle tests, which may include creatine kinase test, MRI, electromyography, and muscle biopsy. Several types of myositis have pulmonary and cardiac manifestations. Treatment is with corticosteroids combined with immunosuppressants and/or IV immune globulin. The cause of autoimmune myositis seems to be an autoimmune reaction to muscle tissue in genetically susceptible people. Familial clustering occurs, and human leukocyte antigen (HLA) subtypes are associated with myositis. For example, the alleles of the 8.1 ancestral haplotype (HLA-DRB1*03-DQA1*05-DQB1*02) increase risk of polymyositis, dermatomyositis, and Overview of Interstitial Lung Disease Interstitial lung diseases are a heterogeneous group of disorders characterized by alveolar septal thickening, fibroblast proliferation, collagen deposition, and, if the process remains unchecked... read more . Possible inciting events include viral myositis and underlying cancer. The association of cancer with dermatomyositis (less so with polymyositis) suggests that a tumor may incite myositis as the result of an...

यह सम्पूर्ण पृष्ठ या इसके कुछ अनुभाग हिन्दी के अतिरिक्त अन्य भाषा(ओं) में भी लिखे गए हैं। आप इनका स्वप्रतिरक्षित रोग वर्गीकरण एवं बाह्य साधन वे रोग स्वप्रतिरक्षित रोग (Autoimmune diseases) कहलाते हैं जिनके होने पर किसी जीव की स्वप्रतिरक्षित रोगों की चिकित्सा में प्रायः दवाओं का उपयोग करके प्रतिरक्षा प्रणाली की सक्रियता को कम किया जाता है जिसे अनुक्रम • 1 मानदण्ड (क्राइटेरिया) • 2 वर्गीकरण • 3 चिकित्सा-विकास • 4 इन्हें भी देखें • 5 अन्य पठनीय सामग्री • 6 सन्दर्भ • 7 इन्हें भी देखें • 8 बाहरी कड़ियाँ मानदण्ड (क्राइटेरिया) [ ] वर्गीकरण [ ] नाम Accepted/ suspected Hypersensitivity I, II, III, IV आटोएन्टीबॉडी टिप्पणी Accepted interferon omega; transglutaminase; aromatic acid carboxylase; Accepted T-cells Accepted Accepted I I Autoimmune Accepted Accepted II complement activation Accepted cell-mediated Accepted Accepted Accepted Accepted Accepted Unknown or multiple Accepted Accepted anti gpIIb-IIIa or 1b-IX Accepted Accepted Balo disease/ immune-mediated systemic vasculitis; linkage to HLA-B51 (HLA-B27); very different manifestations with ulcers as common symptom; also called Morbus Adamandiades-Behçet IgA (elevated in 50% of patients), IgA (in mesangial deposits on kidney biopsy) similar to overlaps both IgG autoantibodies targeting the type XVII collagen component of hemidesmosomes Over expression of Accepted IV?? Suspected similar to Suspected anti-BP-1, anti BP-2 precipitates Accepted II idiopathic or secondary to leukemia or infection III aka Temporal arteritis; involves A...

There are different types of myositis, as follows: Polymyositis Polymyositis (PM) is a rare disease that affects proximal, or core, muscles, such as the back, hips, and neck. This muscle weakness can appear in a matter of days or become apparent over several months. People with PM often have other autoimmune diseases. PM affects fewer than Dermatomyositis Dermatomyositis (DM) also affects the proximal muscles. However, DM causes skin rashes and other skin-related symptoms as well. DM is another rare condition that affects fewer than Juvenile myositis Juvenile myositis (JM) affects children younger than 18 years of age. The condition includes juvenile polymyositis (JPM) and juvenile dermatomyositis (JDM). JPM causes inflammation in the muscles, whereas JDM results in the inflammation in blood vessels. Doctors diagnose around Immune-mediated necrotizing myositis Immune-mediated necrotizing myositis (IMNM) is also known as necrotizing autoimmune myopathy. It has similar symptoms to PM, but IMNM causes necrosis, or muscle cell death. Necrosis can lead to severe muscle weakness on both sides of the body. An estimated In some cases, the cause of IMNM may be due to using certain medications, such as statins. Inclusion body myositis Inclusion body myositis (IBM) causes progressive muscle atrophy and weakness that may affect one side of the body more than the other. IBM most commonly affects people of 50 years of age and older. IBM affects an estimated Infectious myositis Scientist...