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diagnosis pathophysiology 21hydroxylasedeficiency 21ohd algorithm anteriorischemicopticneuropathy cah congenital deficiency diabetes diabeticketoacidosis dka gca genetics giantcellarteritis hydroxylase hyperplasia peds rheumatology signs
Anterior ischemic optic neuropathy (AION) - Recognition of giant cell arteritis (GCA) 1) Is visual loss caused
optic neuropathy (AION ... loss caused by AION ... field: altitudinal defect ... Doppler US : halo sign ... #Rheumatology #Ophthalmology
Congenital Adrenal Hyperplasia - 21-Hydroxylase Deficiency - Signs and Symptoms • Brain: Androgenization effects, Glucocorticoid effects,
Hydroxylase Deficiency - Signs ... and Symptoms • ... Hydroxylase #Deficiency #Signs ... #Symptoms #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 ... maintains appropriate ion ... Signs/Symptoms/Complications ... pathophysiology #genetics #endocrinology ... #peds #pediatrics
Diabetic Ketoacidosis (DKA) - Pathogenesis and Clinical Findings • Note: in DKA, body K+ is lost
patient has good renal ... 3) Follow the anion ... Signs/Symptoms/Complications ... pathophysiology #endocrinology
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