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  2. Lymphedema - Wikipedia

    en.wikipedia.org/wiki/Lymphedema

    Lymphedema is most frequently a complication of cancer treatment or parasitic infections, but it can also be seen in a number of genetic disorders. Tissues with lymphedema are at high risk of infection because the lymphatic system has been compromised. [3] Though incurable and progressive, a number of treatments may improve symptoms. [2]

  3. Waldmann disease - Wikipedia

    en.wikipedia.org/wiki/Waldmann_disease

    Signs and symptoms of the disease include diarrhea, nausea, swelling of the legs, protein-losing enteropathy, immunodeficiency and loss of lymphatic fluid into the intestines. [ 2 ] [ 4 ] It is usually diagnosed before the patient is 3 years old, but it is sometimes diagnosed in adults.

  4. Essential fructosuria - Wikipedia

    en.wikipedia.org/wiki/Essential_fructosuria

    Essential fructosuria is a genetic condition that is inherited in an autosomal recessive manner. [3] Mutations in the KHK gene, located on chromosome 2p23.3-23.2 are responsible. The incidence of essential fructosuria has been estimated at 1:130,000. [4] The actual incidence is likely higher, because those affected are asymptomatic. [citation ...

  5. Edema - Wikipedia

    en.wikipedia.org/wiki/Edema

    Phlebetic lymphedema (or phlebolymphedema) is seen in untreated chronic venous insufficiency and is the most common type of edema (approx. 90%). [14] It is a combination venous/lymphatic disorder that originates in defective "leaky" veins that allows the blood to back flow ( venous reflux ), slowing the return of the blood to the heart ( venous ...

  6. Lymphangiectasia - Wikipedia

    en.wikipedia.org/wiki/Lymphangiectasia

    Lymphangiectasia, also known as "lymphangiectasis", [1] is a pathologic dilation of lymph vessels. [2] When it occurs in the intestines it is known as intestinal lymphangiectasia, colloquially recognized as Waldmann's disease in cases where there is no secondary cause. [3]

  7. Milroy's disease - Wikipedia

    en.wikipedia.org/wiki/Milroy's_disease

    Milroy's disease is also known as primary or hereditary lymphedema type 1A or early onset lymphedema. It is a very rare disease with only about 200 cases reported in the medical literature. Milroy's disease is an autosomal dominant condition caused by a mutation in the FLT4 gene which encodes the vascular endothelial growth factor receptor 3 ...

  8. Fructose malabsorption - Wikipedia

    en.wikipedia.org/wiki/Fructose_malabsorption

    The following list of favorable foods was cited in the paper: "Fructose malabsorption and symptoms of Irritable Bowel Syndrome Guidelines for effective dietary management". [19] The fructose and glucose contents of foods listed on the Australian food standards [23] would appear to indicate that most of the listed foods have higher fructose levels.

  9. Bilateral lower extremity inflammatory lymphedema - Wikipedia

    en.wikipedia.org/wiki/Bilateral_lower_extremity...

    The pathophysiology is not yet well understood. Leukocytoclastic vasculitis is proposed to be the underlying cause resulting in reactive lymphedema. [2] Prolonged standing with full knee extension and minimal movement for a prolonged period of time is postulated to induce a temporary failure in pumping the venous and lymphatic systems in the calf region leading to acute gravity-dependent ...

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