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diagnosis differential management signs causes hematology treatment pediatrics evaluation insufficiency peds psychiatry syndrome 21hydroxylasedeficiency 21ohd anemia anorexianervosa apml bariatric bulimianervosa
Adrenal Insufficiency - Differential Diagnosis Workup Algorithm Primary Adrenal Insufficiency: • Autoimmune primary adrenal insufficiency • Adrenoleukodystrophy,
Differential Diagnosis Workup ... Algorithm Primary ... genetic disorder • CAH ... Differential #Diagnosis #Workup ... #Algorithm #endocrinology
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
of congenital adrenal ... #CAH #algorithm ... treatment #Peds #Endocrinology ... #Adrenal #pathophysiology
Congenital Adrenal Hyperplasia - 21-Hydroxylase Deficiency - Signs and Symptoms • Brain: Androgenization effects, Glucocorticoid effects,
Congenital Adrenal ... Deficiency - Signs and Symptoms ... Cardiovascular: Abnormal ... Deficiency #Signs #Symptoms ... #diagnosis #endocrinology
Short Stature - Differential Diagnosis Algorithm Normal Variant, Normal Puberty Onset (BA = CA) • Familial Short
Differential Diagnosis Algorithm ... Normal Variant ... • Congenital Adrenal ... Differential #Diagnosis #Algorithm ... #endocrinology
Tall Stature - Differential Diagnosis Algorithm Normal Growth (BA=CA) • Familial Tall Stature • XYY Syndrome Obese BMI
Differential Diagnosis Algorithm ... Normal Growth ... (BA=CA) • Familial ... Exogenous Obesity Normal ... #endocrinology
Non-ACS Myocardial Injury - Elevated Troponin Differential Diagnosis and Workup Algorithm • Chronic Myocardial Injury: End
Diagnosis and Workup ... Algorithm • ... Injury: End Stage Renal ... or Normal ... Differential #Diagnosis #Algorithm
Approach to Thyroid Function Tests in the Evaluation of Hyperthyroidism • Low TSH, Low normal T4
• Low TSH, Low normal ... Hyperthyroidism: Work-up ... Can repeat labs ... Hyperthyroidism #algorithm ... #diagnosis #endocrinology
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 ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology
Primary Adrenal Insufficiency: • ACTH stimulation test - Synthetic ACTH does not stimulate cortisol secretion because
production • CRH ... aldosterone - Often normal ... deficiency of CRH ... diagnosis #testing #endocrinology ... #workup
Diabetic Ketoacidosis (DKA) - Pathogenesis and Clinical Findings • Note: in DKA, body K+ is lost
to be falsely normal ... patient has good renal ... Signs/Symptoms/Complications ... DiabeticKetoacidosis #DKA #pathophysiology ... #endocrinology
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