Template:Infobox medical condition/testcases

Bisalbuminemia

Bisalbuminemia (Q4917184) health specialty (P1995)

clinical chemistry

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Bisalbuminemia	Bisalbuminemia

Pneumonia

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Pneumonia Other names pneumonitis, bronchopneumonia A chest X-ray showing a very prominent wedge-shape area of airspace consolidation in the right lung characteristic of bacterial pneumonia. Pronunciation /njuːˈmoʊniə/ Specialty Something-with-ref Symptoms cough, difficulty breathing, rapid breathing, fever Duration few weeks Causes bacteria, virus, aspiration Differential diagnosis COPD, asthma, pulmonary edema, pulmonary embolism Medication antibiotics, steroids, antivirals Frequency 450 million (7%) per year Deaths 4 million per year

Pneumonia Other names pneumonitis, bronchopneumonia A chest X-ray showing a very prominent wedge-shape area of airspace consolidation in the right lung characteristic of bacterial pneumonia. Pronunciation /njuːˈmoʊniə/ Specialty Something-with-ref Symptoms cough, difficulty breathing, rapid breathing, fever Duration few weeks Causes bacteria, virus, aspiration Differential diagnosis COPD, asthma, pulmonary edema, pulmonary embolism Medication antibiotics, steroids, antivirals Frequency 450 million (7%) per year Deaths 4 million per year

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Facioscapulohumeral muscular dystrophy Other names Landouzy–Dejerine muscular dystrophy, FSHMD, FSH Play media Timelapse of DUX4 being expressed in FSHD Muscle Cells Specialty Neurology Symptoms Facial weakness, scapular winging, foot drop Usual onset Adolescence Duration Long term Types FSHD1, FSHD2 Causes Genetic (inherited or new mutation) Diagnostic method Genetic testing Differential diagnosis Limb-girdle muscular dystrophy (especially LGMD2A), Pompe disease, Mitochondrial myopathy, Polymyositis Management Physical therapy, bracing, orthopedic surgery Frequency 1 in 8333 to 1 in 15000

Facioscapulohumeral muscular dystrophy Other names Landouzy–Dejerine muscular dystrophy, FSHMD, FSH Play media Timelapse of DUX4 being expressed in FSHD Muscle Cells Specialty Neurology Symptoms Facial weakness, scapular winging, foot drop Usual onset Adolescence Duration Long term Types FSHD1, FSHD2 Causes Genetic (inherited or new mutation) Diagnostic method Genetic testing Differential diagnosis Limb-girdle muscular dystrophy (especially LGMD2A), Pompe disease, Mitochondrial myopathy, Polymyositis Management Physical therapy, bracing, orthopedic surgery Frequency 1 in 8333 to 1 in 15000