7 results
clinical diagnosis peds physicalexam deficiency differential goiter hypothyroidism otolaryngology thyroid 21hydroxylasedeficiency 21ohd adrenal brudzinskis cah comparison congenitaladrenalhyperplasia genetics hypocalcemia lowcalcium
Thyroid Goiter on Physical Exam Mother and daughter both presenting with thyroid goiters caused by iodine deficiency.
thyroid goiters caused ... by iodine deficiency ... #deficiency #endocrinology ... #clinical #video ... #neck #hypothyroidism
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 Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
#CAH #algorithm ... #causes #pediatrics ... treatment #Peds #Endocrinology ... #Adrenal #pathophysiology
Hypocalcemia - Differential Diagnosis Algorithm - Low and High PTH LOW PTH - Hypoparathyroid - Congenital (Pediatric)
Differential Diagnosis Algorithm ... - Congenital (Pediatric ... Post-operative neck ... Tumor lysis syndrome ... #PTH #endocrinology
Thyroid Goiter on Physical Exam Mother and daughter both presenting with thyroid goiters caused by iodine deficiency.
thyroid goiters caused ... by iodine deficiency ... #deficiency #endocrinology ... #clinical #video ... #neck #hypothyroidism
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 Short Stature - Differential Diagnosis Algorithm Normal Variant, Normal Puberty Onset (BA = CA) • Familial Short
Differential Diagnosis Algorithm ... • Turner Syndrome ... Differential #Diagnosis #Algorithm ... #endocrinology ... #causes #pediatrics
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski) Brudzinski's sign is characterized
Passive neck flexion ... causes spinal cord ... While the pathophysiology ... Video by Dr. ... #PhysicalExam #Pediatrics
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 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 ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
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