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diagnosis 21ohd cryofibrinogenemia dermatology gca genetics giantcell management pathophysiology pediatrics peds rash rheumatology secondary syphilis temporal
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
Giant cell arteritis (GCA) Giant cell arteritis (GCA) definition: Most common systemic inflammatory vasculitis in older adults
Diagnosis = clinical ... systemic sx + signs ... required due to skip ... GCA #Temporal #Signs ... #Symptoms #Diagnosis
Cryofibrinogenemia Summary Cryofibrinogenemia Epidemiology: • 40-70 years with a modest female predominance Cryofibrinogenemia: • The precipitation of a
Cryofibrinogenemia Symptoms ... cryoglobulins • Negative causes ... Biopsy: Typical pathologic ... to medium-sized arteries ... #hematology
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
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