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diagnosis pediatrics primary symptoms 21hydroxylasedeficiency 21ohd adrenal cah causes chloride congenitaladrenalhyperplasia diabetes differential genetics hyperparathyroidism hypochloremia hypothyroid insipidus interpretation myopathy
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
#CAH #algorithm ... CongenitalAdrenalHyperplasia #diagnosis #comparison ... #treatment #Peds ... #Endocrinology ... #Adrenal #pathophysiology
Approach to Thyroid Function Tests in the Evaluation of Hyperthyroidism • Low TSH, Low normal T4
Evaluation of Hyperthyroidism ... Possibly Central Hypothyroidism ... → Signs of ... #algorithm #diagnosis ... #endocrinology
Diabetes Insipidus vs Syndrome of Inappropriate ADH (SIADH) - Comparison Table Diabetes Insipidus - Inadequate ADH SIADH -
ADH (SIADH) - Comparison ... Insipidus #SIADH #Comparison ... #Table #Pathophysiology ... #Signs #Symptoms ... #Diagnosis #Endocrinology
Primary Hyperthyroidism - Pathogenesis and Clinical Findings Note: Although rare, gestational diseases can lead to thyrotoxicosis due
Primary Hyperthyroidism ... Secondary hyperthyroidism ... Signs/Symptoms: ... #endocrinology ... #pathophysiology
Hyperparathyroidism - Primary vs Secondary vs Tertiary Lab Comparison: • Primary Hyperparathyroidism: ↑→PTH, ↑Calcium, ↑Vitamin D,
Tertiary Lab Comparison ... Symptoms: Commonly no signs ... Hyperparathyroidism #diagnosis #endocrinology ... Secondary #Tertiary #pathophysiology
Hypothyroid Myopathy Very common (up to 80% ) in patients with hypothyroidism Pathophysiology: • T4 deficiency leads to
patients with hypothyroidism ... Pathophysiology ... Hypothyroid #Myopathy #pathophysiology ... #signs #symptoms ... #endocrinology
Hypochloremia - Differential Diagnosis Algorithm Cause - Decreased Intake: • Low salt in diet • Exclusive D5W
Differential Diagnosis Algorithm ... - Gitelman SIGNS ... Cl⁻ with other components ... Differential #Diagnosis #Algorithm ... #Pathophysiology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
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