8 results
clinical goiter neck thyroid video hypothyroidism iodine diagnosis mass symptoms 21hydroxylasedeficiency 21ohd addisons cah congenital disease genetics hashimotos hydroxylase hyperplasia
Thyroid Goiter on Physical Exam Mother and daughter both presenting with thyroid goiters caused by iodine deficiency.
goiter moves with swallowing ... Thyroid #Goiter #PhysicalExam ... #iodine #deficiency ... #endocrinology ... hypothyroidism #otolaryngology
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 Retrosternal Thyroid Goiter on Physical Exam Note the movement with swallowing, indicating a thyroid mass. #Retrosternal #Thyroid #Goiter
movement with swallowing ... Thyroid #Goiter #PhysicalExam ... clinical #video #endocrinology ... #neck #mass #otolaryngology
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 Thyroid Goiter in Severe Hypothyroidism on Neck Physical Examination TSH 124. Hashimoto’s, lost to care and thyroid
moves up with swallowing ... Thyroid #Mass #Neck #PhysicalExam ... Hypothyroidism #endocrinology ... #Hashimotos #otolaryngology
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 Endemic Thyroid Goiter on Physical Exam Note the movement of the thyroid mass with swallowing. Dr. Bruno Farnetano
thyroid mass with swallowing ... Thyroid #Goiter #PhysicalExam ... #iodine #deficiency ... #endocrinology ... hypothyroidism #otolaryngology
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 Thyroid Goiter on Physical Exam Mother and daughter both presenting with thyroid goiters caused by iodine deficiency.
goiter moves with swallowing ... Thyroid #Goiter #PhysicalExam ... #iodine #deficiency ... #endocrinology ... hypothyroidism #otolaryngology
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 Primary Adrenal Insufficiency Addison's Disease - Damage of the adrenal glands with lack of cortisol, androgens and
include protein C deficiency ... Aldosterone Deficiency ... Reduced libido • Signs ... addisons #disease #endocrinology ... #diagnosis #signs
Congenital Adrenal Hyperplasia - 21-Hydroxylase Deficiency - Signs and Symptoms • Brain: Androgenization effects, Glucocorticoid effects,
21-Hydroxylase Deficiency ... - Signs and Symptoms ... #Hydroxylase #Deficiency ... #Signs #Symptoms ... #diagnosis #endocrinology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
21-Hydroxylase Deficiency ... 21-OHD in the adrenal ... as "congenital adrenal ... Signs/Symptoms/Complications ... pathophysiology #genetics #endocrinology
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