33 results
diagnosis management differential symptoms syndrome neurology clinical comparison geriatrics physicalexam treatment algorithm cardiology dementia genetics kawasaki newborn summary types video
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
CAH #algorithm #causes ... #pediatrics #CongenitalAdrenalHyperplasia ... comparison #treatment #Peds ... #Endocrinology ... #Adrenal #pathophysiology
Total Anomalous Pulmonary Venous Return (TAPVR) • Introduction • Classification • Pathophysiology of TAPVR • Presentation
Introduction • Classification ... • Pathophysiology ... Classic “snowman sign ... management #cardiology #peds ... #pediatrics #summary
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski) Brudzinski's sign is characterized
Passive neck flexion causes ... While the pathophysiology ... young (less than 2 ... despite severe disease ... #Peds
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 Shock Classification Types - Pathophysiology Comparison Obstructive Shock: • Obstructive shock is characterized by a blockage in
Shock Classification ... Types - Pathophysiology ... in blood flow caused ... Depends on the cause ... advanced valvular disease
Alzheimer’s Disease: Pathogenesis and Clinical Findings Risk factor for Late Onset Alzheimer's (99% of cases): - Increasing
Alzheimer’s Disease ... Presenilin 1 and 2 ... chromosome 21) Signs ... AlzheimersDisease #Dementia #pathophysiology ... #geriatrics #diagnosis
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
disomy: inheriting 2 ... Prader-Willi Syndrome Signs ... Obesity -> Type 2 ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
Multi-System Inflammatory Syndrome in Children (MIS-C) vs. Kawasaki Disease CDC Case Definition for MIS-C; • < 21
Kawasaki Disease ... CDC Case Definition ... hospitalization • >2 ... Comparison #diagnosis #peds ... #pediatrics #COVID19
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Growth Hormone Excess - Pathogenesis and clinical findings • Acromegaly and gigantism share the same pathophysiology
• Other rare causes ... Cardiovascular disease ... Overproduction #diagnosis #signs ... #symptoms #endocrinology ... #pathophysiology
Hashitoxicosis ‘Leakage’ symptoms of active Hashimoto’s disease - Hashitoxicosis (Htx) can occur during the initial hyperthyroid stage in
active Hashimoto’s disease ... thyroiditis that causes ... and scarring 2. ... Hashitoxicosis #Hashimotos #Endocrinology ... #Diagnosis #Pathophysiology
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