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Results 4201 - 4210 of 9113 for Abnormality
  • Retinitis Pigmentosa Diagnosis
    Health - 6 Jul 2023
    Retinitis pigmentosa is commonly identified by the examination of the appearance of the retina using slit lamp biomicroscopy. Common findings on examination and steps in diagnosis include...
  • Acute Lymphoblastic Leukemia Diagnosis
    Health - 6 Jul 2023
    Diagnosis of acute lymphoblastic leukemia is based on laboratory and pathological tests. The first test is usually blood tests. If this indicates abnormalities, further tests are ordered.
  • Bladder Cancer Diagnosis
    Health - 4 Jul 2023
    Bladder cancer may be suspected based on symptoms of the condition such as blood in the urine and the presence of risk factors such as a family history of bladder cancer.
  • Beta-Thalassemia Types
    Health - 4 Jul 2023
    Beta-thalassemia is an inherited disorder of the blood that affects the hemoglobin inside red blood cells. The condition is caused by an abnormality in the production of the beta globin chain found in...
  • Hypophosphatasia Causes
    Health - 17 Jun 2023
    Hypophosphatasia is a rare, inherited metabolic disorder that affects the bones and teeth by disrupting a process called mineralization.
  • Hypophosphatasia Symptoms
    Health - 17 Jun 2023
    Hypophosphatasia is a rare, inherited metabolic disorder that affects the bones and teeth. The condition leads to impaired mineralization, a process where calcium and phosphorus are usually taken up...
  • COVID-19 variants and severity influence heart issues associated with long COVID
    News - 5 Jun 2023
    Patients infected with beta and delta COVID-19 variants, and those who required hospital stays for COVID-19 infection, were more likely to experience heart issues associated with long COVID, according...
  • Phases of Chronic Myeloid Leukemia
    Health - 26 May 2023
    Chronic myeloid leukemia (CML) is a type of cancer that begins in the cells in the bone marrow that are involved in the production of blood cells. The condition can be classified into 3 main phases...
  • Efficient assay system aids rapid genetic diagnosis of mitochondrial diseases
    News - 18 May 2023
    The gene ECHS1 encodes for enoyl-CoA hydratase short-chain 1, a mitochondrial enzyme involved in branched-chain amino acid and fatty acid metabolism.
  • Dyskeratosis Congenita Genetics
    Health - 18 May 2023
    Dyskeratosis congenita is a rare form of bone marrow failure, where the bone marrow fails to produce enough blood cells.

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