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  2. Multiple epiphyseal dysplasia - Wikipedia

    en.wikipedia.org/wiki/Multiple_epiphyseal_dysplasia

    Multiple epiphyseal dysplasia (MED), also known as Fairbank's disease, is a rare genetic disorder (dominant form: 1 in 10,000 births) that affects the growing ends of bones.

  3. Hereditary haemochromatosis - Wikipedia

    en.wikipedia.org/wiki/Hereditary_haemochromatosis

    The condition may be reversible when haemochromatosis is treated and excess iron stores are reduced. Arrhythmia or abnormal heart rhythm can cause heart palpitations, chest pain, and light-headedness, and is occasionally life-threatening. This condition can often be reversed with treatment. [citation needed]

  4. Iron overload - Wikipedia

    en.wikipedia.org/wiki/Iron_overload

    Iron overload (also known as haemochromatosis or hemochromatosis) is the abnormal and increased accumulation of total iron in the body, leading to organ damage. [1] The primary mechanism of organ damage is oxidative stress, as elevated intracellular iron levels increase free radical formation via the Fenton reaction.

  5. List of medical abbreviations - Wikipedia

    en.wikipedia.org/wiki/List_of_medical_abbreviations

    Pronunciation follows convention outside the medical field, in which acronyms are generally pronounced as if they were a word (JAMA, SIDS), initialisms are generally pronounced as individual letters (DNA, SSRI), and abbreviations generally use the expansion (soln. = "solution", sup. = "superior").

  6. Pneumonoultramicroscopicsilicovolcanoconiosis - Wikipedia

    en.wikipedia.org/wiki/Pneumonoultramicroscopicsi...

    ultra: from Latin, meaning beyond; micro and scopic: from ancient Greek, meaning small looking, referring to the fineness of particulates; silico-: from Latin, silicon; volcano: from Latin, referring to volcano; coni: from ancient Greek (κόνις, kónis) which means dust-osis: from ancient Greek, suffix to indicate a medical condition

  7. Hereditary multiple exostoses - Wikipedia

    en.wikipedia.org/wiki/Hereditary_multiple_exostoses

    Medical genetics Hereditary multiple osteochondromas ( HMO ), also known as hereditary multiple exostoses , is a disorder characterized by the development of multiple benign osteocartilaginous masses ( exostoses ) in relation to the ends of long bones of the lower limbs such as the femurs and tibias and of the upper limbs such as the humeri and ...

  8. Sulfhemoglobinemia - Wikipedia

    en.wikipedia.org/wiki/Sulfhemoglobinemia

    Sulfhemoglobinemia is a rare condition in which there is excess sulfhemoglobin (SulfHb) in the blood. The pigment is a greenish derivative of hemoglobin which cannot be converted back to normal, functional hemoglobin. It causes cyanosis even at low blood levels.

  9. List of diagnoses characterized as pseudoscience - Wikipedia

    en.wikipedia.org/wiki/List_of_diagnoses...

    Conditions that are not widely recognized, about which there is an ongoing debate within the scientific and medical literature. Functional disorders are a set of conditions that cannot be explained by structural or biochemical abnormalities. [3] These raise challenges around diagnosis and treatment, with debate around whether they are psychogenic.