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diagnosis peds treatment 21hydroxylasedeficiency chagas disease endocrinology examination hematology hemophagocytic hlh lymphohistiocytosis pathophysiology physicalexam trypanosomiasis
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
deficiencies present in infants ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD ... pathophysiology #genetics ... endocrinology #peds #pediatrics
Newborn Infant - Routine Examination Birthweight, gestational age and birthweight percentile are noted. General observation Of the baby's
Newborn Infant - ... paediatrician or geneticist ... for any midline defects ... #Newborn #Infant ... Examination #Peds #Pediatrics
Hemophagocytic Lymphohistiocytosis (HLH) Definition: Overwhelming clinical syndrome associated with excessive macrophage activation and cytokine storm due to
most frequently affects ... infants < 3 months ... Diagnosis: HLH signs ... and symptoms can ... Lymphohistiocytosis #diagnosis #management
Chagas Disease - American Trypanosomiasis - Diagnosis and Management Summary Chagas disease (American trypanosomiasis) is an infectious
Diagnosis and Management ... Romana's sign ... /symptoms, positive ... q12h)x60 days • Pediatric ... 90-120 days • Pediatric
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