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21hydroxylasedeficiency diagnosis essential genetics hematology management pediatrics peds 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
Essential Thrombocythemia (ET) ET is a chronic myeloproliferative neoplasm. Most cases are related to mutations that affect
Thrombocythemia (ET ... Most cases are related ... , symptoms and complications ... MI, stroke, DVT/ ... Hydroxyurea + anticoagulation
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