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hypothyroid 21hydroxylasedeficiency 21ohd diagnosis genetics hyperthyroidism hypothyroidism myopathy pediatrics peds
Hypothyroid Myopathy Very common (up to 80% ) in patients with hypothyroidism Pathophysiology: • T4 deficiency leads to
Hypothyroid Myopathy ... hypothyroidism Pathophysiology ... #Myopathy #pathophysiology ... #signs #symptoms ... #endocrinology
Hypothyroidism and Hyperthyroidism - Symptoms and Signs Hypothyroidism: - General - From asymptomatic to myxedema coma, “Like
Hyperthyroidism - Symptoms ... and Signs Hypothyroidism ... #Hyperthyroid # ... Symptoms #Signs ... #Diagnosis #endocrinology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... vomiting • Late (shock ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology
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