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MEDIMYST: Unveiling Rare Organ Diseases ( / @medimyst ) MediMyst explores the often-unheard world of rare organ diseases, empowering patients with clear explanations and fostering a supportive community. We translate complex medical jargon, illuminate hidden symptoms, and offer the latest research. Join us and become a champion for rare disease awareness. #RareDiseases #MedicalMysteries #PatientSupport #Empowerment #HopeForRareDiseases #JoinTheFight #UnderstandingHealth https://www.digistore24.com/content/3... LAM - "Embark on a journey unraveling the mysteries of This text is a preview for a video about Lymphangioleiomyomatosis (LAM), a very rare lung disease. The video will explore the complexities of LAM, including: What causes it (etiology) Who it affects (epidemiology) The symptoms (clinical manifestations) How it's managed (treatment options) By watching, you'll gain a deeper understanding of this debilitating disease. 1. What are Lung Diseases? Lung diseases are conditions that affect the structures and function of the lungs, impairing their ability to exchange oxygen and carbon dioxide effectively. While many lung diseases, such as asthma or pneumonia, are relatively common, there are some rare conditions that affect a small number of people. 2. Understanding Rare Lung Diseases: Rare lung diseases refer to those that have a low prevalence rate and may have complex mechanisms. These conditions often require specialized medical care and extensive research to fully comprehend. 3. The Rarest Lung Disease: Among the rare lung diseases, one of the rarest is called lymphangioleiomyomatosis (LAM). LAM primarily affects women and is characterized by an abnormal growth of smooth muscle cells in the lungs, leading to the formation of cystic lesions. These cystic lesions impair lung function, making breathing more difficult over time. The prevalence of LAM (https://www.thelamfoundation.org/) is estimated at 3.4 – 7.8 per million women, although the true prevalence is probably much higher. 4. Causes of LAM: The exact cause of LAM is not fully understood, but researchers have identified a connection to mutations in the tuberous sclerosis complex (TSC) genes. TSC genes play a role in regulating cell growth and division, and when mutated, they can lead to the development of LAM. 5. Signs and Symptoms: The symptoms of LAM can vary from person to person. Some common signs include shortness of breath, chest pain, coughing, and fatigue. These symptoms may worsen over time, potentially leading to more severe respiratory problems. 6. Diagnosis: Diagnosing LAM usually involves analyzing a combination of medical history, physical examinations, lung function tests, imaging studies (such as CT scans), and a lung biopsy. Due to the rarity of the disease, it is essential to consult with specialists in pulmonary medicine for an accurate diagnosis. 7. Treatment Options: Currently, there is no cure for LAM, but management strategies can help relieve symptoms and slow disease progression. Treatment options may include medications to improve lung function, such as bronchodilators or hormonal therapies. In some cases, lung transplantation may be considered for severe cases. 8. Living with LAM: Living with LAM can be challenging, but with proper medical management and lifestyle adjustments, individuals with LAM can lead fulfilling lives. Engaging in regular physical activity, managing stress, and maintaining a healthy diet can help maintain overall well-being. 9. Research and Future Directions: Understanding rare lung diseases like LAM is an ongoing process. Scientists and medical professionals continue to investigate the underlying mechanisms and explore potential treatment options. Research advancements may pave the way for improved diagnostic tools and targeted therapies in the future. Summary: LAM is one of the rarest lung diseases, mainly affecting women. While living with LAM can be difficult, patients are not alone. Medical professionals, researchers, and support networks are working to improve awareness, treatments, and quality of life for those with LAM and other rare lung diseases. Summarize the text below “Conclusion: Lymphangioleiomyomatosis (LAM) is one of the rarest lung diseases, primarily affecting women. Although living with a rare lung disease can be challenging, it is crucial for individuals with LAM to know that they are not alone. Medical professionals, researchers, and patient support networks are working together to improve awareness, treatments, and ultimately, the quality of life for those affected by LAM and other rare lung diseases. References: 1. Lymphangioleiomyomatosis (LAM). (n.d.). National Organization for Rare Disorders. Retrieved December 10, 2023, from https://rarediseases.org/rare-disease...