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21hydroxylasedeficiency diagnosis et genetics glftap hematology macroadenoma management masseffects mnemonic pediatrics peds pituitary sideeffects thrombocythemia
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
Pituitary Mass Effects - Pathogenesis and Clinical Findings • Pituitary turnors are almost always a benign
order of least-essential ... to most essential ... Signs / Symptoms ... #SideEffects #endocrinology ... mnemonic #GLFTAP #pathophysiology
Essential Thrombocythemia (ET) ET is a chronic myeloproliferative neoplasm. Most cases are related to mutations that affect
Essential Thrombocythemia ... Most cases are related ... MI, stroke, DVT/ ... Hydroxyurea + anticoagulation ... EricsMedicalLectures/ #Essential
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