enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Schistosomiasis - Wikipedia

    en.wikipedia.org/wiki/Schistosomiasis

    Schistosomiasis, also known as snail fever, bilharzia, and Katayama fever [1] [2] [9] is a disease caused by parasitic flatworms called schistosomes. [5] It affects the urinary tract or the intestines. [5] Symptoms include abdominal pain, diarrhea, bloody stool, or blood in the urine. [5]

  3. Schistosoma japonicum - Wikipedia

    en.wikipedia.org/wiki/Schistosoma_japonicum

    Historical accounts of Katayama disease dates back to the discovery of S. Japonicum in Japan in 1904. The disease was named after an area it was endemic to, Katayama district, Hiroshima, Japan. [11] If left untreated, it will develop into a chronic condition characterized by hepatosplenic disease and impaired physical and cognitive development.

  4. Congenital disorder of glycosylation - Wikipedia

    en.wikipedia.org/wiki/Congenital_disorder_of...

    Mannose supplementation relieves the symptoms in MPI-CDG for the most part, [39] even though the hepatic fibrosis may persist. [40] Fucose supplementation has had a partial effect on some SLC35C1-CDG patients. [41] In 2024, it was reported that a study suggested that Ibuprofen might be helpful as a treatment for one such genetic disease. [42]

  5. Cerebellar ataxia, neuropathy, vestibular areflexia syndrome

    en.wikipedia.org/wiki/Cerebellar_ataxia...

    Cerebellar ataxia with neuropathy and vestibular areflexia syndrome (CANVAS) is an autosomal recessive late-onset heredodegenerative multisystem neurological disease. The symptoms include poor balance and difficulty walking. Chronic cough and difficulty swallowing may also be present.

  6. Kagami-Ogata Syndrome - Wikipedia

    en.wikipedia.org/wiki/Kagami-Ogata_Syndrome

    Kagami-Ogata syndrome is a rare genetic disease that is caused by mutations on Maternal chromosome 14 or by paternal UPD(14). [1] The main signs of this disease are: polyhydramnios , narrow bell-shaped thorax , coat-hanger-like ribs , abdominal wall defect , enlarged placenta . [ 2 ]

  7. Mother who lost only son to rare COVID complication warns ...

    www.aol.com/lifestyle/mother-lost-only-son-rare...

    It shares symptoms with toxic shock and Kawasaki disease, including fever, rashes, swollen glands, conjunctivitis and, in severe cases, heart inflammation, and can cause multiple organ failure ...

  8. Felty's syndrome - Wikipedia

    en.wikipedia.org/wiki/Felty's_syndrome

    Felty's syndrome (FS), also called Felty syndrome, [1] is a rare autoimmune disease characterized by the triad of rheumatoid arthritis, enlargement of the spleen and low neutrophil count. The condition is more common in those aged 50–70 years, specifically more prevalent in females than males, and more so in Caucasians than those of African ...

  9. Löffler's syndrome - Wikipedia

    en.wikipedia.org/wiki/Löffler's_syndrome

    Löffler's syndrome is a disease in which eosinophils accumulate in the lung in response to a parasitic infection. The parasite can be Ascaris , Strongyloides stercoralis , or Dirofilaria immitis [ 1 ] which can enter the body through contact with the soil. [ 2 ]