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  2. Microvillous inclusion disease - Wikipedia

    en.wikipedia.org/wiki/Microvillous_inclusion_disease

    Microvillus inclusion disease, previously known as Davidson's disease, congenital microvillus atrophy and, less specifically, microvillus atrophy (note: microvillus is often misspelled as microvillous), is a rare genetic disorder of the small intestine that is inherited in an autosomal recessive pattern.

  3. Pappenheimer bodies - Wikipedia

    en.wikipedia.org/wiki/Pappenheimer_bodies

    They are a type of inclusion body composed of ferritin aggregates, or mitochondria or phagosomes containing aggregated ferritin. They appear as dense, blue-purple granules within the red blood cell and there are usually only one or two, located in the cell periphery.

  4. Infantile digital fibromatosis - Wikipedia

    en.wikipedia.org/wiki/Infantile_digital_fibromatosis

    Infantile digital fibromatosis (IDF), also termed inclusion body fibromatosis or Reye's tumor, usually occurs as a single, small, asymptomatic, nodule in the dermis on a finger or toe [1] of infants and young children. [2] IMF is a rare disorder with approximately 200 cases reported in the medical literature as of 2021. [3]

  5. Apparent mineralocorticoid excess syndrome - Wikipedia

    en.wikipedia.org/wiki/Apparent_mineralocorticoid...

    Apparent mineralocorticoid excess is an autosomal recessive [2] disorder causing hypertension (high blood pressure), hypernatremia (increased blood sodium concentration) and hypokalemia (decreased blood potassium concentration).

  6. Molar incisor hypomineralisation - Wikipedia

    en.wikipedia.org/wiki/Molar_Incisor_Hypominerali...

    Molar incisor hypomineralisation (MIH) is a type of enamel defect affecting, as the name suggests, the first molars and incisors in the permanent dentition. [1] MIH is considered a worldwide problem with a global prevalence of 12.9% and is usually identified in children under 10 years old. [2]

  7. Menkes disease - Wikipedia

    en.wikipedia.org/wiki/Menkes_disease

    Occipital horn syndrome (sometimes called X-linked cutis laxa or Ehlers-Danlos type 9 [10]) is a mild form of Menkes syndrome that begins in early to middle childhood. It is characterized by calcium deposits in a bone at the base of the skull ( occipital bone ), coarse hair, and loose skin and joints.

  8. US FDA proposes standardized testing to detect asbestos in ...

    www.aol.com/news/us-fda-proposes-standardized...

    The healthcare giant seeks to resolve the claims through an approximately $10 billion settlement in bankruptcy. It has denied the allegations and called its products safe.

  9. Hypervitaminosis - Wikipedia

    en.wikipedia.org/wiki/Hypervitaminosis

    In the United States, overdose exposure to all formulations of "vitamins" (which includes multi-vitamin/mineral products) was reported by 62,562 individuals in 2004 with nearly 80% of these exposures in children under the age of 6, leading to 53 "major" life-threatening outcomes and 3 deaths (2 from vitamins D and E; 1 from a multivitamin with ...