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diagnosis differential physicalexam clinical dementia genetics newborn symptoms video workup 21hydroxylasedeficiency 21ohd adrenal alzheimersdisease anomalous bilirubinemia brudzinskis cah cardiology comparison
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
#CAH #algorithm ... #causes #pediatrics ... 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
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 ... #Jaundice #Algorithm
Causes of Common Accidental and Non-Accidental Pediatric Fractures - Differential Diagnosis Algorithm Accidental Trauma - Distal Radius
Causes of Common ... Non-Accidental Pediatric ... Fracture • < 2 ... #Causes #Peds # ... Pediatrics
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
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
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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 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
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 ... Workup #Diagnosis #Geriatrics
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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