25 results
diagnosis peds neurology summary syndrome treatment cardiogenic cardiology disease genetics pulmonary 21hydroxylasedeficiency 21ohd algorithm als alzheimersdisease amyotrophic anomalous aortoenteric bullous
Cardiogenic Shock: Pathogenesis, complications and clinical findings #Cardiogenic #Shock #pathophysiology #cardiology #diagnosis #signs #symptoms
Cardiogenic Shock ... #Cardiogenic #Shock ... #pathophysiology ... cardiology #diagnosis #signs ... #symptoms
Clinical features of shock from dehydration in an infant Decreased level of consciousness Sunken fontanelle Dry mucous
Clinical features of shock ... #PhysicalExam #Signs ... #Symptoms #Shock ... Dehydration #Peds #Pediatrics
Pediatric SVT - Management Algorithm Identify SVT: • HR not variable • Abrupt rate changes • Infants:
Pediatric SVT - ... Management Algorithm ... Signs of shock or ... #tachycardia #Management ... Algorithm #peds #Pediatric
Alzheimer’s Disease: Pathogenesis and Clinical Findings Risk factor for Late Onset Alzheimer's (99% of cases): - Increasing
chromosome 21) Signs ... / Symptoms / Complications ... AlzheimersDisease #Dementia #pathophysiology ... #geriatrics #diagnosis ... #signs #symptoms
Pathophysiology and Clinical Manifestations of Shock #Shock #Manifestations #Cardiogenic #Hypovolemic #Signs #Symptoms
Pathophysiology ... Manifestations of Shock ... #Shock #Manifestations ... #Hypovolemic #Signs ... #Symptoms
Total Anomalous Pulmonary Venous Return (TAPVR) • Introduction • Classification • Pathophysiology of TAPVR • Presentation
Classification • Pathophysiology ... Classic “snowman sign ... Pre-Operative Management ... Post-Operative Management ... cardiology #peds #pediatrics
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome Signs ... /Symptoms/Complications ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
Pott's Disease in Tuberculosis - Diagnosis and Management Summary Epidemiology: - Typically from TB endemic areas -
Diagnosis and Management ... cases Clinical Signs ... years - May have signs ... /symptoms of active ... decreased reflexes Pathophysiology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... vomiting • Late (shock ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds #pediatrics
PECARN Head CT Decision Aid The Head CT Choice decision aid was developed in Rochester, Minnesota. Full
observation, and signs ... and symptoms that ... (Figure 2) #Management ... PatientInfo #Peds #Pediatrics
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