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diagnosis endocrinology management nephrology pediatrics 21hydroxylasedeficiency 21ohd algorithm cah calcifications causes clincial comparison congenitaladrenalhyperplasia crisis encephalopathy genetics infant lipiduria nejm
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
of congenital adrenal ... comparison #treatment #Peds ... Endocrinology #Adrenal ... #pathophysiology
Plain radiography of the abdomen revealed calcification of both adrenal glands. A homozygous mutation in LIPA
calcification of both adrenal ... calcification of the adrenal ... #clincial #peds ... #adrenal #calcifications ... #infant #NEJM #Wolmans
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
21-OHD in the adrenal ... as "congenital adrenal ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds
Posterior Reversible Encephalopathy Syndrome (PRES) Overview Clinico-Radiological Syndrome, characterized by: • Headache • Seizures • Altered mental
Immunosuppressive agents, Renal ... Etiology: • Pathophysiology ... Seizures: Treat with AEDs
Lipiduria Pathophysiology 1) Damaged glomerular basement membrane allows plasma lipids to escape into Bowman's space and enter
Lipiduria Pathophysiology ... to escape into Bowman's ... are absorbed by renal ... #Lipiduria #Pathophysiology
Scleroderma Renal Crisis (SRC) Clinical Presentation of Scleroderma Renal Crisis: 1) Acute kidney injury 2) Abrupt onset of hypertension 3)
Scleroderma Renal ... of Scleroderma Renal ... anemia (MAHA) Pathophysiology ... Monitoring • Renal ... , add other BP meds
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