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diagnosis differential pathophysiology pediatrics 21hydroxylasedeficiency 21ohd acth amyloidosis cah comparison congenitaladrenalhyperplasia genetics gout hyperuricemia insufficiency stimulation tallstature test treatment uricacid
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
of congenital adrenal ... #CAH #algorithm ... #causes #pediatrics ... comparison #treatment #Peds ... #Endocrinology
Hyperuricemia - Differential Diagnosis Algorithm Primary - Over-production • Increased turnover of nucleotides Primary
Differential Diagnosis Algorithm ... • Chronic renal ... Differential #Diagnosis #Algorithm ... #endocrinology ... #causes
Adrenal Insufficiency Diagnosis Algorithm - Evaluation of HPA Axis Response to ACTH Early am cortisol < 3
Diagnosis Algorithm ... Response to ACTH Early ... unclear (often the case ... Insufficiency #Diagnosis #Algorithm ... Stimulation #Test #Endocrinology
Tall Stature - Differential Diagnosis Algorithm Normal Growth (BA=CA) • Familial Tall Stature • XYY Syndrome Obese BMI
Differential Diagnosis Algorithm ... • Congenital Adrenal ... Tall Stature (Early ... #endocrinology ... #causes
Amyloidosis - Summary Group of disorders associated with extracellular deposition of fibrils formed from low-molecular-weight proteins in
Manifestations: Renal ... • Can detect early ... protein-albumin" dissociation ... in urine • Amyloid ... hypoadrenalism • Nausea
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... 21-OHD in the adrenal ... Hypoglycemia • Early ... pathophysiology #genetics #endocrinology ... #peds #pediatrics
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