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Mendelson's syndrome, named in 1946 for American obstetrician and cardiologist Curtis Lester Mendelson, is a form of chemical pneumonitis or aspiration pneumonitis caused by aspiration of stomach contents (principally gastric acid) during anaesthesia in childbirth.
Curtis Lester Mendelson (September 4, 1913 - October 13, 2002) was an obstetrician and American cardiologist. Mendelson's syndrome was named after him in 1946. [1] [2]
Mendelson's syndrome is a type of chemical pneumonitis. Mineral oil should not be given internally to young children, pets, or anyone with a cough, hiatal hernia, or nocturnal reflux, because it can cause complications such as lipoid pneumonia. [3] Due to its low density, it is easily aspirated into the lungs, where it cannot be removed by the ...
Fish acute toxicity syndrome; Fitz-Hugh–Curtis syndrome; Fitzsimmons–Guilbert syndrome; Flammer syndrome; Fleischer's syndrome; Floating–Harbor syndrome; Floppy eyelid syndrome; Floppy trunk syndrome; Florid cutaneous papillomatosis; Flynn–Aird syndrome; Foal immunodeficiency syndrome; Foerster's syndrome; Foix–Alajouanine syndrome ...
Hamman's syndrome, also known as Macklin's syndrome, is a syndrome of spontaneous subcutaneous emphysema [1] (air in the subcutaneous tissues of the skin) and pneumomediastinum (air in the mediastinum, the center of the chest cavity), sometimes associated with pain and, less commonly, dyspnea (difficulty breathing), dysphonia, and a low-grade fever.
There are many mimics that present with similar symptoms, such as vocal cord dysfunction, cardiac arrhythmias, cardiomyopathies, and gastroesophageal reflux disease. It is also important to distinguish those who have asthma with exercise worsening, and who consequently will have abnormal testing at rest, from true exercise-induced ...
Jamie Lee Curtis is celebrating an important milestone: 25 years of sobriety. The Oscar winner, 65, recently took to Instagram to mark more than two decades of sobriety. “25 years clean and sober.
Hutchinson-Gilford progeroid syndrome (HGPS) is an extremely rare autosomal dominant genetic disorder in which symptoms resembling aspects of aging are manifested at an early age. [8] Its occurrence is usually the result of a sporadic germline mutation ; although HGPS is genetically dominant, people rarely live long enough to have children ...