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diagnosis clinical differential physicalexam symptoms algorithm cardiology dementia genetics geriatrics management newborn treatment video 21hydroxylasedeficiency 21ohd a4c acromegaly adhd adrenal
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
Approach to Neonatal Jaundice Causes of pathologic hyperbilirubinemia can be classified as due to (1) increased bilirubin
Neonatal Jaundice Causes ... non-hemolytic processes), (2) ... #Diagnosis #Peds ... #Pediatrics #Neonatal ... #Differential #Workup
Total Anomalous Pulmonary Venous Return (TAPVR) • Introduction • Classification • Pathophysiology of TAPVR • Presentation
Introduction • Classification ... • Pathophysiology ... Classic “snowman sign ... management #cardiology #peds ... #pediatrics #summary
Major neurocognitive disorders (MNCD): Diagnosis and workup 1) Clinical diagnosis Cognitive impairment + loss of autonomy 2)
loss of autonomy 2) ... Alzheimer - 1st cause ... (parkinsonian signs ... Differential #Subtypes #Classification ... #Geriatrics #Workup
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
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 ... #PhysicalExam #Pediatrics ... #Peds
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 Alzheimer’s Disease: Pathogenesis and Clinical Findings Risk factor for Late Onset Alzheimer's (99% of cases): - Increasing
Presenilin 1 and 2 ... chromosome 21) Signs ... AlzheimersDisease #Dementia #pathophysiology ... #geriatrics #diagnosis ... #signs #symptoms
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
Causes of Secondary Hypertension - Workup and Differential Diagnosis Approach (when evaluation should be done): 1. Severe or
Hypertension - Workup ... hypertension and signs ... renal bruit or signs ... Vasculitis • Endocrinologic ... #Hypertension #Workup
Acute Otitis Media: Pathogenesis and Clinical Findings (in Children) Upper Respiratory Tract Infection: - Bacterial: Streptococcus
- 2/3 both bacterial ... #OtitisMedia #pathophysiology ... diagnosis #symptoms #signs ... #peds #pediatrics
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