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  2. Da Costa's syndrome - Wikipedia

    en.wikipedia.org/wiki/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 .

  3. Erythrokeratodermia variabilis - Wikipedia

    en.wikipedia.org/wiki/Erythrokeratodermia_variabilis

    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

  4. List of syndromes - Wikipedia

    en.wikipedia.org/wiki/List_of_syndromes

    Supernumerary nipples–uropathies–Becker's nevus syndrome; Supernumerary phantom limb; Survivor syndrome; Susac's syndrome; Sweet's syndrome; Swyer–James syndrome; Syndrome of inappropriate antidiuretic hormone secretion; Syndrome of subjective doubles; Syndrome Without A Name; HHH syndrome; Systemic inflammatory response syndrome; Sézary ...

  5. Jacob Mendes Da Costa - Wikipedia

    en.wikipedia.org/wiki/Jacob_Mendes_Da_Costa

    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 ...

  6. Mouth and genital ulcers with inflamed cartilage syndrome

    en.wikipedia.org/wiki/Mouth_and_genital_ulcers...

    The median time interval between the onset of symptoms and the diagnosis was 6 years, with a range of 26 days to 14 years. This suggests that the symptoms of MAGIC syndrome may manifest relatively long after the initial onset of symptoms. During the course of MAGIC syndrome, the signs and symptoms of BD may typically occur before those of RP. [4]

  7. Cerebellar ataxia, neuropathy, vestibular areflexia syndrome

    en.wikipedia.org/wiki/Cerebellar_ataxia...

    Cerebellar ataxia with neuropathy and vestibular areflexia syndrome (CANVAS) is an autosomal recessive late-onset heredodegenerative multisystem neurological disease. The symptoms include poor balance and difficulty walking. Chronic cough and difficulty swallowing may also be present.

  8. Autosomal dominant multiple pterygium syndrome - Wikipedia

    en.wikipedia.org/wiki/Autosomal_dominant...

    Autosomal dominant multiple pterygium syndrome; Other names: Distal arthrogryposis type 8 [1] Autosomal dominant multiple pterygium syndrome is inherited in an autosomal dominant fashion. Specialty: Dermatology

  9. List of eponymous diseases - Wikipedia

    en.wikipedia.org/wiki/List_of_eponymous_diseases

    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 ...