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21hydroxylasedeficiency diagnosis endocrinology genetics lung pathophysiology pediatrics signs
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical Findings ... enzyme 21-OHase causes ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD ... endocrinology #peds
Lung Findings on Physical Exam Crackles: • Short, discontinuous, sounds mostly heard during inspiration • Caused by
Lung Findings on ... alveoli as seen in pulmonary ... Bronchophony: • "Say ... #Pulmonary #PhysicalExam ... #diagnosis #signs
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