3 results
21hydroxylasedeficiency adrenal cah congenital diagnosis eyelid genetics graefes graves hydroxylase hyperplasia hyperthyroidism ophthalmology ophthalmopathy pathophysiology pediatrics peds signs von vongraefes
Von Graefe's Sign - Graves' Eyelid Ophthalmopathy on Ocular Exam Lagging of the upper eyelid on downward
Von Graefe's Sign ... - Graves' Eyelid ... #Graves #Eyelid ... #PhysicalExam # ... ophthalmology #endocrinology
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 21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
21-Hydroxylase Deficiency ... amount of enzyme deficiency ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD ... pathophysiology #genetics #endocrinology
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
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