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management differential signs symptoms nephrology rheumatology syndrome classification disease insufficiency peds physicalexam primary renal secondary workup algorithm barre complications encephalopathy
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
#CAH #algorithm ... #causes #pediatrics ... #comparison #treatment ... #Peds #Endocrinology ... #Adrenal #pathophysiology
Primary Adrenal Insufficiency Addison's Disease - Damage of the adrenal glands with lack of cortisol, androgens and
aldosterone Causes ... cause adrenal calcification ... Serum DHEAS Diagnosis ... addisons #disease #endocrinology ... #diagnosis #signs
Primary Adrenal Insufficiency: • ACTH stimulation test - Synthetic ACTH does not stimulate cortisol secretion because
ACTH stimulation test ... aldosterone - Low in cases ... - This test can ... Evaluation #laboratory #diagnosis ... #testing #endocrinology
Congenital Adrenal Hyperplasia - 21-Hydroxylase Deficiency - Signs and Symptoms • Brain: Androgenization effects, Glucocorticoid effects,
Hydroxylase Deficiency - Signs ... rest tumor formation ... Hydroxylase #Deficiency #Signs ... #Symptoms #diagnosis ... #endocrinology
Short Stature - Differential Diagnosis Algorithm Normal Variant, Normal Puberty Onset (BA = CA) • Familial Short
- Differential Diagnosis ... • Congenital Adrenal ... Panhypopituitarism Treatment ... #Algorithm #endocrinology ... #causes #pediatrics
Adrenal Insufficiency - Diagnosis and Management Summary Primary Adrenal Insufficiency: Most Common Cause in the US: Autoimmune Adrenalitis Other
: Most Common Cause ... Adrenalitis Other causes ... A STIM test can ... ACTH STIM TEST: ... #Management #Endocrinology
Hematuria - Differential Diagnosis Framework Gross Hematuria: Red/Dark urine • 1ml blood/liter urine can induce color change
- Differential Diagnosis ... hematuria • Signs ... → Diagnostic of ... #causes #urology ... #nephrology #renal
Romberg's Test for Proprioception History: First described in the 19th century in patients with tabes dorsalis (later
Romberg's Test for ... (Romberg's sign ... Observe when patient closes ... disease: standing can ... #neurology #diagnosis
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Myasthenia Gravis Overview Myasthenia Gravis is an autoimmune disorder of the postsynaptic neuromuscular junction. Ab to
Bedside: ice pack test ... /Edrophonium test ... - Cogan sign ... - Peek sign 2. ... #management #neurology
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