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21hydroxylasedeficiency 21ohd diagnosis disease genetics management pathophysiology treatment trypanosomiasis
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
also known as "congenital ... Signs/Symptoms/Complications ... pathophysiology #genetics #endocrinology ... #peds #pediatrics
Chagas Disease - American Trypanosomiasis - Diagnosis and Management Summary Chagas disease (American trypanosomiasis) is an infectious
Romana's sign ... Indeterminate form (No signs ... /symptoms, positive ... transfusions), congenital ... IFA) assays to detect
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