29 results
diagnosis peds video physicalexam symptoms goiter neck signs thyroid bronchoscopy hypothyroidism laryngoscopy deficiency geriatrics iodine dementia genetics laryngomalacia management mass
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
algorithm #causes #pediatrics ... treatment #Peds #Endocrinology ... #Adrenal #pathophysiology
Thyroid Goiter in Severe Hypothyroidism on Neck Physical Examination TSH 124. Hashimoto’s, lost to care and thyroid
#PhysicalExam #clinical ... Hypothyroidism #endocrinology ... #Hashimotos #otolaryngology
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 Thyroid Goiter on Physical Exam Mother and daughter both presenting with thyroid goiters caused by iodine deficiency.
iodine #deficiency #endocrinology ... #clinical #video ... hypothyroidism #otolaryngology
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 Retrosternal Thyroid Goiter on Physical Exam Note the movement with swallowing, indicating a thyroid mass. #Retrosternal #Thyroid #Goiter
#PhysicalExam #clinical ... #video #endocrinology ... #neck #mass #otolaryngology
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 Aortic Stenosis & Bicuspid Aortic Valve (AS) • Introduction & Pathophysiology • Classifications • Epidemiology •
Introduction & Pathophysiology ... Epidemiology • Clinical ... cardiology #peds #pediatrics
Alzheimer's Disease - Summary • Epidemiology • Pathophysiology • Risk Factors • Presentation • Diagnosis •
Epidemiology • Pathophysiology ... Treatment • Clinical ... diagnosis #management #geriatrics
Primary Hyperthyroidism - Pathogenesis and Clinical Findings Note: Although rare, gestational diseases can lead to thyrotoxicosis due
Pathogenesis and Clinical ... Hyperthyroidism #endocrinology ... #pathophysiology
Graves’ Disease: Pathogenesis and Clinical Findings B & T lymphocyte mediated autoimmunity attack TSH receptor -> Continuous
Pathogenesis and Clinical ... GravesDisease #pathophysiology ... #endocin #endocrinology
Growth Hormone Excess - Pathogenesis and clinical findings • Acromegaly and gigantism share the same pathophysiology
Pathogenesis and clinical ... share the same pathophysiology ... signs #symptoms #endocrinology ... #pathophysiology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
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