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neck thyroid clinical goiter hypothyroidism physicalexam deficiency differential diagnosis pediatrics peds 21hydroxylasedeficiency 21ohd algorithm genetics head hyperthyroidism lowthyroid mass pathophysiology
Web chart of various etiologies related to congenital neck masses. #differential #causes #pediatrics #congenital #neck #head #masses
neck masses. ... #differential #causes ... #pediatrics #congenital ... #neck #head #masses ... #otolaryngology
Thyroid Goiter on Physical Exam Mother and daughter both presenting with thyroid goiters caused by iodine deficiency.
thyroid goiters caused ... #deficiency #endocrinology ... #clinical #video ... #neck #hypothyroidism ... #otolaryngology
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 Pemberton's Sign caused by a Retrosternal Thyroid Goiter Elevating the arms causes the previously flat neck veins
Pemberton's Sign caused ... Elevating the arms causes ... PhysicalExam #clinical #video ... #mass #SVC #Syndrome ... #otolaryngology
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 Thyroid Goiter on Physical Exam Mother and daughter both presenting with thyroid goiters caused by iodine deficiency.
thyroid goiters caused ... #deficiency #endocrinology ... #clinical #video ... #neck #hypothyroidism ... #otolaryngology
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 Endemic Thyroid Goiter on Physical Exam Note the movement of the thyroid mass with swallowing. Dr. Bruno Farnetano
of the thyroid mass ... #PhysicalExam #iodine ... #clinical #video ... #neck #hypothyroidism ... #otolaryngology
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 Hyperthyroidism Overview Clinical Manifestation of Hyperthyroidism: • Fatigue • Weight loss • Heat intolerance • Depression, nervousness
Hyperdefecation • Anterior neck ... Toxicosis • Iodine ... Thionamide - Iodine ... hyperthyroidism #causes ... #differential #endocrinology
Hypothyroidism - Differential Diagnosis Algorithm Central Hypothyroidism • Isolated TSH Deficiency • Panhypopituitarism Thyroid Hormone Resistance Iatrogenic Primary Hypothyroidism -
Hemosiderosis - Congenital ... • Severe Iodine ... Diagnosis #Algorithm #endocrinology ... #causes
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
mutation in CYP21A2 coding ... enzyme 21-OHase causes ... also known as "congenital ... be labeled as males ... pathophysiology #genetics #endocrinology
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