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21hydroxylasedeficiency diagnosis differential edema genetics noncardiogenic pediatrics peds pulmonary
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology ... #genetics #endocrinology
Uncommon Causes of Noncardiogenic Pulmonary Edema (NCPE) - Differential Diagnosis Framework High Altitude Pulmonary Edema: • Accumulation
Pulmonary Edema (NCPE ... blood cells in the lung ... capillaries • Criteria ... • Signs/Symptoms ... • Signs/Symptoms
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