16 results
diagnosis algorithm management cardiology symptoms differential disease genetics hepatology kawasaki physicalexam treatment 21hydroxylasedeficiency 21ohd abscess adrenal anomalous anomaly arthritis brudzinskis
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
algorithm #causes #pediatrics ... comparison #treatment #Peds ... #Endocrinology ... #Adrenal #pathophysiology
Pediatric SVT - Management Algorithm Identify SVT: • HR not variable • Abrupt rate changes • Infants:
Pediatric SVT - ... HR > 220bpm • Children ... - Older children ... Signs of shock or ... Management #Algorithm #peds
Acute Otitis Media: Pathogenesis and Clinical Findings (in Children) Upper Respiratory Tract Infection: - Bacterial: Streptococcus
Clinical Findings (in Children ... pressure => Negative ... #OtitisMedia #pathophysiology ... diagnosis #symptoms #signs ... #peds #pediatrics
Ebstein Anomaly • Prevalence • Pathophysiology • Presentation • Physical Examination Findings • Initial Management •
Prevalence • Pathophysiology ... • Surgery in Children ... management #cardiology #pediatrics ... #peds
Kawasaki Disease (Mucocutaneous Lymph Node Syndrome) An rare systemic acute febrile vasculitic syndrome. Aetiology unknown. Affects
Affects children ... Disease #Features #Signs ... Symptoms #Diagnosis #Peds ... #Pediatrics
Rapid Assessment of the Neonate With Sonography (RANS) Scan Recommended algorithm for RANS scan. * Abnormal vital
Abnormal vital signs ... #RANS #RAPID #POCUS ... Sonography #Neonate #Peds ... #Pediatrics #Neonatology
Total Anomalous Pulmonary Venous Return (TAPVR) • Introduction • Classification • Pathophysiology of TAPVR • Presentation
Classification • Pathophysiology ... Classic “snowman sign ... management #cardiology #peds ... #pediatrics #summary
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome Signs ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski) Brudzinski's sign is characterized
Brudzinski’s Sign ... Brudzinski's sign ... While the pathophysiology ... #PhysicalExam #Pediatrics ... #Peds
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