4 results
diagnosis 21ohd arteritis dermatology gca genetics giantcell hyperthyroidism management pathophysiology pediatrics peds rash secondary syphilis temporal thyroid
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... enzyme 21-OHase causes ... Signs/Symptoms/Complications ... cold & mottled skin ... a scrotum #21HydroxylaseDeficiency
Secondary Syphilis Rash Secondary syphilis is the most contagious of all the stages of this disease, and
Skin rash and malaise ... The signs and symptoms ... resembling rashes caused ... Rash #Diagnosis #Clinical ... #Photo #Dermatology
Hyperthyroidism Overview Clinical Manifestation of Hyperthyroidism: • Fatigue • Weight loss • Heat intolerance • Depression, nervousness
Hyperthyroidism Overview Clinical ... Thickening of skin ... hyperthyroidism #causes ... #endocrinology ... #signs #symptoms
Giant cell arteritis (GCA) Giant cell arteritis (GCA) definition: Most common systemic inflammatory vasculitis in older adults
Diagnosis = clinical ... systemic sx + signs ... very remarkable w/differential ... required due to skip ... GCA #Temporal #Signs
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