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✅ What are the signs and symptoms of Cystic Fibrosis? Cystic fibrosis signs and symptoms vary, depending on the severity of the disease. Even in the same person, symptoms may worsen or improve as time passes. Some people may not experience symptoms until their teenage years or adulthood. People who are not diagnosed until adulthood usually have milder disease and are more likely to have atypical symptoms, such as recurring bouts of an inflamed pancreas (pancreatitis), infertility and recurring pneumonia. People with cystic fibrosis have a higher-than-normal level of salt in their sweat. Parents often can taste the salt when they kiss their children. Most of the other signs and symptoms of CF affect the respiratory system and digestive system. Respiratory signs and symptoms The thick and sticky mucus associated with cystic fibrosis clogs the tubes that carry air in and out of your lungs. This can cause signs and symptoms such as: A persistent cough that produces thick mucus (sputum) Wheezing Exercise intolerance Repeated lung infections Inflamed nasal passages or a stuffy nose Recurrent sinusitis Digestive signs and symptoms The thick mucus can also block tubes that carry digestive enzymes from your pancreas to your small intestine. Without these digestive enzymes, your intestines can't completely absorb the nutrients in the food you eat. The result is often: Foul-smelling, greasy stools Poor weight gain and growth Intestinal blockage, particularly in newborns (meconium ileus) Chronic or severe constipation, which may include frequent straining while trying to pass stool, eventually causing part of the rectum to protrude outside the anus (rectal prolapse) ✅ What are the complications of Cystic Fibrosis? Complications of cystic fibrosis can affect the respiratory, digestive and reproductive systems, as well as other organs. Respiratory system complications Damaged airways (bronchiectasis)- Cystic fibrosis is one of the leading causes of bronchiectasis, a chronic lung condition with abnormal widening and scarring of the airways (bronchial tubes). This makes it harder to move air in and out of the lungs and clear mucus from the bronchial tubes. Growths in the nose (nasal polyps)- Because the lining inside the nose is inflamed and swollen, it can develop soft, fleshy growths (polyps). Chronic infections- Thick mucus in the lungs and sinuses provides an ideal breeding ground for bacteria and fungi. People with cystic fibrosis may often have sinus infections, bronchitis or pneumonia. Infection with bacteria that is resistant to antibiotics and difficult to treat is common. Coughing up blood (hemoptysis)- Bronchiectasis can occur next to blood vessels in the lungs. The combination of airway damage and infection can result in coughing up blood. Often this is only a small amount of blood, but it can also be life-threatening. ----------------------------------------------------------------------------------------------- Mera Physio - Physiotherapy & Pain Clinic is a chain of physiotherapy clinics across India. If your condition is not treatable at home then visit any of our Physiotherapy clinics. We have more than 100 clinics across India. All our partner locations can be viewed at - https://www.meraphysio.com/ You can also do a video call session with our Physiotherapists. Appointments are available within 48 hours. Call us at (+91) 7470606369 Book online appointment at http://www.meraphysio.com/book-appoin... 👉 Mera Physio main branch: Mera Physio - Physiotherapy & Pain Clinic A-131, Narayan Plaza, Bilaspur (C.G.) - 495004 India Ph: (+91) 7470606369 ----------------------------------------------------------------------------------------------- #CysticFibrosisTreatment #CysticFibrosis #WhatisCysticFibrosis #cyst #lungs #lungdisease #lungdiseases #physiotherapytreatment #physiotherapy #exercises #rehab #rehabilitation