Category: W

  • Wheezy

    Making a whistling sound when breathing.  

  • Wheeze

    A whistling noise in the bronchi. Abnormal high-pitched sound heard through a stethoscope in an airway blocked by mucus, neoplasm, muscle spasm, or pressure. It occurs in asthma, in chronic bronchitis, and unilaterally in the presence of a foreign body or neoplasm in the airway. Audible whistling breath sound often associated with asthma or airway…

  • Wharton’s jelly

    A jelly-like tissue in the umbilical cord. The mesoderm tissue of the umbilical cord, which becomes converted to a loose jellylike mesenchyme surrounding the umbilical blood vessels. The gelatinous intercellular material of the umbilical cord; it consists of collagen, mucin, and hyaluronic acid. It is rich in hyaluronic acid, and in primitive stem cells.  

  • Wharton’s duct

    A duct which takes saliva into the mouth from the salivary glands under the lower jaw [After Thomas Wharton (1614-73), English physician and anatomist at St Thomas’s Hospital, London, UK]. The secretory duct of the submandibular salivary gland. The channel from the salivary gland located under the lower jaw that transports saliva into the mouth.…

  • Wet beriberi

    Beriberi in which the body swells with oedema.  

  • Wet

    Not dry, covered in liquid.  

  • West Nile fever

    A mosquito-borne viral infection which causes fever, pains, enlarged lymph nodes and sometimes inflammation of the brain.  

  • Wertheim’s operation

    A surgical operation to remove the uterus, the lymph nodes which are next to it and most of the vagina, the ovaries and the Fallopian tubes, as treatment for cancer of the uterus [Described 1900. After Ernst Wertheim (1864-1920), Austrian gynaecologist.] A surgical procedure to remove the entire uterus and as much of the surrounding…

  • Werner’s syndrome

    An inherited disorder involving premature ageing, persistent hardening of the skin, underdevelopment of the sex organs and cataracts. Werner syndrome (WS) is an autosomal recessive genetic disease that resembles premature aging (University of Washington, 2000). A genetic mutation on Chromosome 8, labeled WRN, is the cause of WS (National Institutes of Health [NIH], 1997). Although…

  • Werdnig-Hoffmann disease

    A disease in which the spinal muscles atrophy, making the muscles of the shoulders, arms and legs weak. In its most severe form, infants are born floppy, have feeding and breathing problems and rarely live more than two or three years. Werdnig-Hoffmann disease (also known as infantile spinal muscular atrophy Type I, or SMA I)…