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A hiatal hernia or hiatus hernia [2] is a type of hernia in which abdominal organs (typically the stomach) slip through the diaphragm into the middle compartment of the chest. [1] [3] This may result in gastroesophageal reflux disease (GERD) or laryngopharyngeal reflux (LPR) with symptoms such as a taste of acid in the back of the mouth or heartburn.
Gall stones, Diverticulosis, Hiatus hernia: Samter's triad (also known as Acetylsalicylic acid triad or Widal's triad [citation needed] or Francis' triad [citation needed] or Aspirin triad) Aspirin sensitivity, Nasal polyps, Asthma: Aspirin-exacerbated respiratory disease: Tetany in Children - Triad: Stridor, Carpopedal spasm, Convulsions: Tetany
[6] [7] Kinsbourne named the syndrome after his mentor, British neurologist Paul Sandifer, who had initially cared for the patients described in Kinsbourne's case reports. [ 8 ] [ 9 ] [ 10 ] See also
A laparoscopic hernia repair is when the hiatal hernia is corrected using a covering for the mesh that is used to repair the weakened area. The defect is then measured and the mesh is stapled into place. [6] A benefit of performing Laparoscopic hernia repair is shorter recovery times compared to other methods.
Galloway–Mowat syndrome is usually an autosomal recessive disorder, [1] which means the defective gene responsible for the disorder is located on an autosome, and two copies of the defective gene (one inherited from each parent) are required in order to be born with the disorder.
In one report 10% of 100 people investigated for iron deficiency anemia had a large hiatal hernia. [3] A 1967 review found that 20% of 1305 individuals having surgery for hiatal hernia were anemic. [4] Cameron in 1976 [5] compared 259 people with large hiatal hernias visible on chest x-ray with 259 controls without hernias. Present or past ...
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