Ms. A is a 32-year-old woman who presents with a history of systemic lupus erythematosus (SLE) diagnosed 5 years ago. She complains of increasing joint pain and stiffness, particularly in her hands and knees. She also reports fatigue, occasional fever, and a facial rash that worsens with sun exposure. Ms. A has been compliant with her hydroxychloroquine therapy but admits to occasional non-adherence due to gastrointestinal upset. She denies any recent infections or significant changes in her overall health. Clinical Examination: On examination, Ms. A appears fatigued but is alert and oriented. She has a malar rash across her cheeks and nose. There are no signs of oral ulcers. Joint examination reveals tenderness and swelling of the proximal interphalangeal joints bilaterally, with decreased range of motion due to pain. Cardiovascular and respiratory examinations are unremarkable. Laboratory Findings: Complete blood count: Mild normocytic anemia (hemoglobin 11.8 g/dL), normal white blood cell count and platelet count. Urinalysis: Proteinuria (1+), no hematuria. Antinuclear antibodies (ANA): Positive, with a titer of 1:1280. Anti-dsDNA antibodies: Positive. Complement levels (C3 and C4): Low. What is the probable diagnosis?
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A patient reports sudden onset of pain, warmth, and swelling…
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What is the standard of care for croup treatment:
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In girls, the first appearance of breast buds is termed:
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Physical activity enhances cognitive development.
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