13 results
diagnosis pediatrics management cardiogenic genetics syndrome 21hydroxylasedeficiency 21ohd acquired agammaglobulinemia cap cardiology childhood community complications cop cryptogenic cystitis dehydration emphysematous
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
Complications of Measles: Pathogenesis and Clinical Findings • ADEM -> Fever, headache, neck stiffness, BBD, mental
Pericarditis • Pneumonia ... Complications #diagnosis #signs ... #symptoms #pathophysiology
Community Acquired Pneumonia - Presenting Features • History in favor of CAP: Dyspnea, Cough, particularly if
Community Acquired Pneumonia ... complicated by septic shock ... criteria: Septic shock ... #diagnosis #signs ... #symptoms
Pathophysiology and Clinical Manifestations of Shock #Shock #Manifestations #Cardiogenic #Hypovolemic #Signs #Symptoms
Pathophysiology ... Manifestations of Shock ... #Shock #Manifestations ... #Hypovolemic #Signs ... #Symptoms
Childhood Immunization Schedule: Why we immunize • Diphtheria Toxin -> URT inflammation causes pseudomembrane with hardened
hemorrhagic rash; symptoms ... of shock • Mumps ... non-specific viral symptoms ... #Immunization #peds ... #pediatrics #pathophysiology
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
Acute Otitis Media: Pathogenesis and Clinical Findings (in Children) Upper Respiratory Tract Infection: - Bacterial: Streptococcus
Streptococcus pneumoniae ... #OtitisMedia #pathophysiology ... #diagnosis #symptoms ... #signs #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 ... vomiting • Late (shock ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds
Cryptogenic Organizing Pneumonia - Illness Script PATHOPHYSIOLOGY: Unknown trigger, reversible inflammatory/fibroproliferative process. Polypoid fibroblastic aggregates that plug
Illness Script PATHOPHYSIOLOGY ... Males=Females SIGNS ... /SYMPTOMS: • Acute ... misdiagnosed as CAP • Symptoms ... identified (autoimmune, meds
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