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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 ...
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 ...
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 ...
XLP syndrome X-linked lymphoproliferative syndrome (see Duncan Disease) XLSA X-linked sideroblastic anemia: XMEA X-linked myopathy with excessive autophagy: XMEN X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia XP Xeroderma pigmentosa: XSCID X-linked severe combined immunodeficiency: XXX syndrome ...
Da Costa's syndrome; Carbon monoxide poisoning: Chest pain, along with symptoms like headache, dizziness, nausea, and confusion, can occur as a result of carbon monoxide poisoning, which is often mistaken for the flu due to its nonspecific presentation [38]
Other names: Progressive symmetric erythrokeratodermia, Gottron type: Erythrokeratodermia variabilis is inherited in an autosomal dominant manner of inheritance: Specialty: Dermatology, medical genetics Usual onset: Infancy
The following is a list of genetic disorders and if known, type of mutation and for the chromosome involved. Although the parlance "disease-causing gene" is common, it is the occurrence of an abnormality in the parents that causes the impairment to develop within the child.