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symptoms 21hydroxylasedeficiency 21ohd causes diagnosis differential genetics hypothyroid myopathy pediatrics peds primary thyroid
Primary Hyperthyroidism - Pathogenesis and Clinical Findings Note: Although rare, gestational diseases can lead to thyrotoxicosis due
Primary Hyperthyroidism ... Pathogenesis and Clinical ... Signs/Symptoms: ... #endocrinology ... #pathophysiology
Hypothyroid Myopathy Very common (up to 80% ) in patients with hypothyroidism Pathophysiology: • T4 deficiency leads to
patients with hypothyroidism ... Pathophysiology ... fibers Spectrum of Clinical ... #signs #symptoms ... #endocrinology
Hyperthyroidism Overview Clinical Manifestation of Hyperthyroidism: • Fatigue • Weight loss • Heat intolerance • Depression, nervousness
Hyperthyroidism ... Overview Clinical ... Thickening of skin ... #differential #endocrinology ... #signs #symptoms
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... Signs/Symptoms/Complications ... cold & mottled skin ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology
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