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Da Costa's syndrome, also known as soldier's heart among other names, was a syndrome or a set of symptoms similar to those of heart disease. These include fatigue upon exertion, shortness of breath, palpitations, sweating, chest pain, and sometimes orthostatic intolerance. It was originally thought to be a cardiac condition, and treated with a ...
Da Costa's syndrome; Daentl Townsend Siegel syndrome; Dahlberg Borer Newcomer syndrome; Dandy–Walker syndrome; De Barsy syndrome; de Clérambault's syndrome; De Quervain syndrome; De Winter syndrome; Dead arm syndrome; Deficiency of the interleukin-1–receptor antagonist; Degenerative disc disease; Dejerine–Roussy syndrome; Delayed sleep ...
Jacob Mendes Da Costa, or Jacob Mendez Da Costa (February 7, 1833, Saint Thomas, Danish Virgin Islands, Caribbean – September 12, 1900) was an American physician.. He is particularly known for discovering Da Costa's syndrome (also known as soldier's heart), an anxiety disorder combining effort fatigue, dyspnea, a sighing respiration, palpitation and sweating that he first observed in ...
Mendes da Costa syndrome; Mendes da Costa type erythrokeratodermia; Mutilating keratoderma of Vohwinkel; Mutilating palmoplantar keratoderma; Mutilating palmoplantar keratoderma of the Gamborg–Nielsen type; Mutilating palmoplantar keratoderma with periorificial keratotic plaques; Mutilating palmoplantar keratoderma with periorificial plaques
Print/export Download as PDF; Printable version; In other projects ... 509 "Mendes da Costa syndrome", [3] "Mendes da Costa type erythrokeratodermia", ...
An eponymous disease is a disease, disorder, condition, or syndrome named after a person, usually the physician or other health care professional who first identified the disease; less commonly, a patient who had the disease; rarely, a literary character who exhibited signs of the disease or an actor or subject of an allusion, as characteristics associated with them were suggestive of symptoms ...
Rothmund-Thompson syndrome; Dyskeratosis congenita; Mendes da Costa syndrome; Other hereditary causes; Degos-Touraine syndrome; Diffuse and macular atrophic dermatosis; Hereditary sclerosing poikiloderma of weary; Kindler syndrome; Xeroderma pigmentosum; Acquired; Injury to cold, heat, ionizing radiation, exposure to sensitizing chemicals ...
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