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endocrinology diagnosis hypothyroidism thyroid deficiency goiter neck otolaryngology physicalexam differential 21hydroxylasedeficiency 21ohd autoimmune disease genetics graves interpretation lowthyroid management pathophysiology
Thyroid Goiter on Physical Exam Mother and daughter both presenting with thyroid goiters caused by iodine deficiency.
thyroid goiters caused ... by iodine deficiency ... #PhysicalExam #iodine ... endocrinology #clinical ... #video #neck #hypothyroidism
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 Approach to Thyroid Function Tests in the Evaluation of Hyperthyroidism • Low TSH, Low normal T4
Evaluation of Hyperthyroidism ... Possibly Central Hypothyroidism ... of pregnancy, critical ... → Radioactive Iodine ... #algorithm #diagnosis
Hyperthyroidism Overview Clinical Manifestation of Hyperthyroidism: • Fatigue • Weight loss • Heat intolerance • Depression, nervousness
Overview Clinical ... Toxicosis • Iodine ... with radioactive iodine ... Thionamide - Iodine ... • Radioactive iodine
Graves Disease - Autoimmune Hyperthyroidism Epidemiology: Most common cause of hyperthyroidism, Incidence peaks at 30-50 Diagnosis: 1 )
Epidemiology: Most common cause ... of hyperthyroidism ... Clinical Presentation ... : • Hyperthyroidism ... • Radioactive iodine
Thyroid Goiter on Physical Exam Mother and daughter both presenting with thyroid goiters caused by iodine deficiency.
thyroid goiters caused ... by iodine deficiency ... #PhysicalExam #iodine ... endocrinology #clinical ... #video #neck #hypothyroidism
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 Hypothyroidism - Differential Diagnosis Algorithm Central Hypothyroidism • Isolated TSH Deficiency • Panhypopituitarism Thyroid Hormone Resistance Iatrogenic Primary Hypothyroidism -
Hypothyroidism - ... Differential Diagnosis Algorithm ... • Severe Iodine ... Differential #Diagnosis #Algorithm ... endocrinology #causes
Endemic Thyroid Goiter on Physical Exam Note the movement of the thyroid mass with swallowing. Dr. Bruno Farnetano
#PhysicalExam #iodine ... endocrinology #clinical ... #video #neck #hypothyroidism
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 21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... mutation in CYP21A2 coding ... enzyme 21-OHase causes ... endocrinology #peds
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