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Da Costa's syndrome. 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 ...
Progressive symmetric erythrokeratodermia, Gottron type. Erythrokeratodermia variabilis is inherited in an autosomal dominant manner of inheritance. Specialty. Dermatology, medical genetics. Usual onset. Infancy. Erythrokeratodermia variabilis (also known as " erythrokeratodermia figurata variabilis ", " keratosis extremitatum progrediens ...
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 ...
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 fictional character who exhibited signs of the disease or an actor or subject of a literary allusion, as characteristics associated with them were suggestive of ...
Poikiloderma. Poikiloderma is a skin condition that consists of areas of hypopigmentation, hyperpigmentation, telangiectasias and atrophy . Poikiloderma of Civatte is most frequently seen on the chest or the neck, characterized by red colored pigment on the skin that is commonly associated with sun damage. [ 1]
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 ...
In simple terms, Angelman syndrome is a rare genetic disorder that causes developmental delays, speech problems, and a happy, excitable demeanor. "Other common signs and symptoms usually appear in ...
Gianotti–Crosti syndrome ( / dʒəˈnɒti ˈkrɔːsti / ), also known as infantile papular acrodermatitis, [1] papular acrodermatitis of childhood, [1] and papulovesicular acrolocated syndrome, [2] : 389 is a reaction of the skin to a viral infection. [3] Hepatitis B virus [4] and Epstein–Barr virus are the most frequently reported pathogens.