3 results
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
wasting crisis & hyperkalemia ... Complications: • Hyperkalemia ... decr feeding, weight ... pathophysiology #genetics #endocrinology ... #peds #pediatrics
Causes of Growth Discrepancy: Large for Gestational Age - Differential Diagnosis Algorithm
Maternal Factors:
 • Multiparity
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Gestational Age - Differential ... Diagnosis Algorithm ... • Excessive weight ... Shoulder dystocia • Birth ... Causes #Obstetrics #OBGyn
Malignant Adrenal Mass - Differential Diagnosis Algorithm
Suggestive of Malignancy: Inhomogenous Density, Delay in CT Contrast Washout
Adrenal Mass - Differential ... Diagnosis Algorithm ... to Liver on TI Weighted ... Hypertension +/- Hypokalemia ... #Endocrinology