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  2. Cystic fibrosis - Wikipedia, the free encyclopedia

    en.wikipedia.org/wiki/Cystic_fibrosis

    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.

  3. Distal intestinal obstruction syndrome - Wikipedia

    en.wikipedia.org/wiki/Distal_intestinal...

    Differentiation of DIOS from constipation is generally performed by a unit specializing in the treatment of cystic fibrosis. Adequate hydration and an aggressive regimen of laxatives are essential for treatment and prevention of DIOS. Osmotic laxatives such as polyethylene glycol are preferred. [1]

  4. Fibrosing colonopathy - Wikipedia

    en.wikipedia.org/wiki/Fibrosing_colonopathy

    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]

  5. Exocrine pancreatic insufficiency - Wikipedia

    en.wikipedia.org/wiki/Exocrine_pancreatic...

    Exocrine pancreatic insufficiency (EPI) is the inability to properly digest food due to a lack or reduction of digestive enzymes made by the pancreas.EPI can occur in humans and is prevalent in many conditions [1] such as cystic fibrosis, [2] Shwachman–Diamond syndrome, [3] different types of pancreatitis, [4] multiple types of diabetes mellitus (Type 1 and Type 2 diabetes), [5] advanced ...

  6. Cystic fibrosis–related diabetes - Wikipedia

    en.wikipedia.org/wiki/Cystic_fibrosis–related...

    Cystic fibrosis related diabetes mellitus (CFRD) develops with age, and the median age at diagnosis is 21 years. [1] It is an example of type 3c diabetes – diabetes that is caused by damage to the pancreas from another disease or condition.

  7. Cystic fibrosis transmembrane conductance regulator - Wikipedia

    en.wikipedia.org/wiki/Cystic_fibrosis_trans...

    These are the symptoms of cystic fibrosis, a genetic disorder; however, ΔF508 is not the only mutation that causes this disorder. [ 37 ] Being a heterozygous carrier (having a single copy of ΔF508) results in decreased water loss during diarrhea because malfunctioning or absent CFTR proteins cannot maintain stable ion gradients across cell ...

  8. Idiopathic pulmonary fibrosis - Wikipedia

    en.wikipedia.org/wiki/Idiopathic_pulmonary_fibrosis

    Symptoms typically include gradual onset of shortness of breath and a dry cough. [1] Other changes may include feeling tired, and clubbing abnormally large and dome shaped finger and toenails. [1] Complications may include pulmonary hypertension, heart failure, pneumonia or pulmonary embolism. [1] The cause is unknown, hence the term idiopathic ...

  9. Age of onset - Wikipedia

    en.wikipedia.org/wiki/Age_of_onset

    The age of onset is the age at which an individual acquires, develops, or first experiences a condition or symptoms of a disease or disorder. For instance, the general age of onset for the spinal disease scoliosis is "10-15 years old," [ 1 ] meaning that most people develop scoliosis when they are of age between ten and fifteen years.