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Qué (quién) es Peutz-Jeghers syndrome - definición
AUTOSOMAL DOMINANT GENETIC DISORDER CHARACTERIZED BY THE DEVELOPMENT OF BENIGN HAMARTOMATOUS POLYPS IN THE GASTROINTESTINAL TRACT AND HYPERPIGMENTED MACULES ON THE LIPS AND ORAL MUCOSA (MELANOSIS)
Peutz-Jeghers; Polyps-and-Spots syndrome; Hamartomatous intestinal polyposis; Polyposis, hamartomatous intestinal; Polyps-and-spots syndrome; Peutz-jeghers syndrome; Peutz-Jegher's syndrome; Peutz jeger; Jeghers-Peutz syndrome; Peutz-Jeghers syndrome; Polyposis hamartomatous intestinal; Peutz jegher; Peutz-jegher; Peutz-Jeghers polyp
![[[Micrograph]] of '''Peutz-Jeghers''' type [[colonic polyp]]. [[H&E stain]].](https://commons.wikimedia.org/wiki/Special:FilePath/Peutz-Jeghers syndrome polyp.jpg?width=200 "[[Micrograph]] of '''Peutz-Jeghers''' type [[colonic polyp]]. [[H&E stain]].")
Peutz–Jeghers syndrome
Peutz–Jeghers syndrome (often abbreviated PJS) is an autosomal dominant genetic disorder characterized by the development of benign hamartomatous polyps in the gastrointestinal tract and hyperpigmented macules on the lips and oral mucosa (melanosis). This syndrome can be classed as one of various hereditary intestinal polyposis syndromes and one of various hamartomatous polyposis syndromes.
Reye's syndrome
SYNDROME CHARACTERIZED BY ACUTE BRAIN DAMAGE AND LIVER FUNCTION PROBLEMS
Reyes Syndrome; Reye Syndrome; Reye's Syndrome; Reyes syndrome; Reye’s Syndrome; Reye hepatocerebral syndrome; Rye syndrome; Reye s syndrome; Reye's s syndrome; Reye's syndrome; Reye’s syndrome
['re?z, 'r??z]
¦ noun a life-threatening metabolic disorder in young children, of uncertain cause.
Origin
1960s: named after the Australian paediatrician Ralph D. K. Reye.
Frey's syndrome
HUMAN DISEASE
Auriculotemporal syndrome; Frey syndrome
Frey's syndrome (also known as Baillarger's syndrome, Dupuy's syndrome, auriculotemporal syndrome, or Frey-Baillarger syndrome) is a rare neurological disorder resulting from damage to or near the parotid glands responsible for making saliva, and from damage to the auriculotemporal nerve often from surgery.
Wikipedia
Peutz–Jeghers syndrome
Peutz–Jeghers syndrome (often abbreviated PJS) is an autosomal dominant genetic disorder characterized by the development of benign hamartomatous polyps in the gastrointestinal tract and hyperpigmented macules on the lips and oral mucosa (melanosis). This syndrome can be classed as one of various hereditary intestinal polyposis syndromes and one of various hamartomatous polyposis syndromes. It has an incidence of approximately 1 in 25,000 to 300,000 births.
