• Thumbnail for Myoglobinuria
    Myoglobinuria is the presence of myoglobin in the urine, which usually results from rhabdomyolysis or muscle injury. Myoglobin is present in muscle cells...
    6 KB (545 words) - 03:13, 21 December 2023
  • Thumbnail for Rhabdomyolysis
    quantity of myoglobin exceeds the binding capacity of haptoglobin. Myoglobinuria, the presence of myoglobin in the urine, occurs when the level in plasma...
    49 KB (4,816 words) - 02:56, 18 January 2024
  • Thumbnail for Hemoglobinuria
    microscopically despite a positive dipstick test suggests hemoglobinuria or myoglobinuria. The medical term for RBCs in the urine is hematuria. Hematuria Deters...
    3 KB (180 words) - 08:40, 23 January 2024
  • Thumbnail for Cytochrome c oxidase subunit I
    deficiency, colorectal cancer, sensorineural deafness, and recurrent myoglobinuria. In humans, the MT-CO1 gene is located from nucleotide pairs 5904 to...
    39 KB (4,496 words) - 03:10, 6 January 2024
  • Thumbnail for Cytochrome c oxidase subunit III
    optic neuropathy, mitochondrial complex IV deficiency, and recurrent myoglobinuria . The MT-CO3 gene produces a 30 kDa protein composed of 261 amino acids...
    21 KB (2,391 words) - 01:43, 18 January 2024
  • Thumbnail for Lactate dehydrogenase
    Mutations of the M subunit have been linked to the rare disease exertional myoglobinuria (see OMIM article), and mutations of the H subunit have been described...
    42 KB (4,795 words) - 16:44, 3 April 2024
  • Thumbnail for Glycogen storage disease type V
    previous episodes of myoglobinuria and 6.8% had normal CK (including those with fixed muscle weakness); so an absence of myoglobinuria and normal CK should...
    54 KB (6,261 words) - 05:21, 29 April 2024
  • Thumbnail for Proteinuria
    Interstitial nephritis Sickle cell disease Hemoglobinuria Multiple myeloma Myoglobinuria Organ rejection: Ebola virus disease Nail–patella syndrome Familial...
    21 KB (2,144 words) - 18:16, 31 December 2023
  • Myofibrillar lysis Myofibroblastic tumors Myoglobinuria dominant form Myoglobinuria recurrent Myoglobinuria Myokymia Myoneurogastrointestinal encephalopathy...
    28 KB (2,469 words) - 16:00, 15 March 2024
  • Thumbnail for Carnitine palmitoyltransferase II deficiency
    males. CPT II deficiency is also the most frequent cause of hereditary myoglobinuria. The three main types of carnitine palmitoyltransferase II deficiency...
    26 KB (3,166 words) - 14:52, 27 October 2023