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Cystic fibrosis (also known as CF or mucoviscidosis) is an autosomal recessive genetic disorder affecting most critically the lungs, and also the pancreas, liver, and intestine.
Fibrosing colonopathy is a disease that arises in people with cystic fibrosis treated with high doses of pancreatic enzyme supplements. [1] [2] Symptoms are non-specific with abdominal pain, abdominal swelling, vomiting, and constipation. [1]
Signs and symptoms of DIOS include a sudden onset of crampy abdominal pain, vomiting, and a palpable mass (often in the right lower quadrant) in the abdomen. The characteristic abdominal pain is typically located in the center or right lower quadrant of the abdomen. [ 1 ]
Cystic Fibrosis Research Institute has implemented strategies to increase awareness in underrepresented populations. [38] Though there is ongoing research about cystic fibrosis in underrepresented populations, many of the studies leave much to be desired and are not performed to the standards of studies conducted in white patients.
Symptoms: Shortness of breath, rapid breathing, bluish skin coloration, chest pain, loss of speech [1] Complications: Blood clots, Collapsed lung (pneumothorax), Infections, Scarring (pulmonary fibrosis) [2] Usual onset: Within a week [1] Diagnostic method: Adults: PaO 2 /FiO 2 ratio of less than 300 mm Hg [1] Children: oxygenation index > 4 [3 ...
The abnormal amount of anion secretion causes a reduced amount of ductal water flow. Because of this, the duct's protein concentration increases and causes the duct lumina to get plugged. The onset of cystic fibrosis affects the pancreas more than any other organ (even before birth). [3]
Adult-onset Still's disease [4] ... Cystic fibrosis [4] Epidermolysis ... Schnitzler syndrome [4] Symptoms. Signs and symptoms of amyloidosis can vary depending on ...
The differential diagnosis includes other types of lung disease that cause similar symptoms and show similar abnormalities on chest radiographs. Some of these diseases cause fibrosis, scarring or honeycomb change. The most common considerations include: chronic hypersensitivity pneumonitis; non-specific interstitial pneumonia; sarcoidosis