19 results
diagnosis peds psychiatry behavioraldisorder management cardiogenic differential disease genetics kawasaki neurology syndrome 21hydroxylasedeficiency 21ohd abnormal acutepe adhd als alzheimersdisease amyotrophic
Cardiogenic Shock: Pathogenesis, complications and clinical findings #Cardiogenic #Shock #pathophysiology #cardiology #diagnosis #signs #symptoms
Cardiogenic Shock ... complications and clinical ... #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 from dehydration ... #PhysicalExam #Signs ... #Symptoms #Shock ... Dehydration #Peds #Pediatrics
Diagnostic Algorithm for Suspected Pulmonary Embolism Well's Criteria for PE • Clinical Signs and Symptoms of DVT
Diagnostic Algorithm ... Embolism Well's Criteria ... for PE • Clinical ... Signs and Symptoms ... AcutePE #Diagnosis #Algorithm
Pathophysiology and Clinical Manifestations of Shock #Shock #Manifestations #Cardiogenic #Hypovolemic #Signs #Symptoms
Pathophysiology ... and Clinical Manifestations ... of Shock #Shock ... #Hypovolemic #Signs ... #Symptoms
Alzheimer’s Disease: Pathogenesis and Clinical Findings Risk factor for Late Onset Alzheimer's (99% of cases): - Increasing
Pathogenesis and Clinical ... chromosome 21) Signs ... AlzheimersDisease #Dementia #pathophysiology ... #geriatrics #diagnosis ... #signs #symptoms
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical ... Prader-Willi Syndrome Signs ... /Symptoms/Complications ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
Major Depressive Disorder (MDD): Pathogenesis and Clinical Findings Symptoms (included in DSM 5 criteria) - Present during
Pathogenesis and Clinical ... Findings Symptoms ... included in DSM 5 criteria ... MoodDisorders #Diagnosis #Pathophysiology ... #Signs #Symptoms
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... Signs/Symptoms/Complications ... vomiting • Late (shock ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds #pediatrics
Evaluation of suspected incomplete Kawasaki Disease 1. AHA consensus recommendations 2. Infants ≤6 months old on day ≥7
if they have no clinical ... purposes of this algorithm ... those >day 10 with clinical ... and lab signs ( ... Diagnosis #Peds #Pediatrics
Kawasaki Disease: Clinical Findings Diagnostic Criteria - Fever and 4/5 of the following: • Conjunctivitis • Polymorphous
Kawasaki Disease: Clinical ... Findings Diagnostic Criteria ... hands & feet Signs ... #Diagnosis #Pathophysiology ... #Signs #Symptoms
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