14 results
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
Measles (Rubeola) 
Clinical 
 • High fever 
 • Cough, Coryza, Conjunctivitis (The 3 C's)
comrnon) • Pneumonia ... #KoplikSpots #Features ... #Symptoms #Signs
Community Acquired Pneumonia - Presenting Features
 • History in favor of CAP: Dyspnea, Cough, particularly if
Community Acquired Pneumonia ... - Presenting Features ... criteria: Septic shock ... #diagnosis #signs ... #symptoms
Clinical Features and Complications of Measles

Rash:
Spreads downwards, from behind the ears to the whole Of the
Clinical Features ... Kopliks KoplikSpots #Peds ... Pediatrics #Timeline #Signs ... #Symptoms
Kawasaki Disease (Mucocutaneous Lymph Node Syndrome) 
An rare systemic acute febrile vasculitic syndrome. Aetiology unknown. 
Affects
Kawasaki #Disease #Features ... #Signs #Symptoms ... #Diagnosis #Peds
Low O2 saturation that does not respond to supplemental O2
- Key diagnostic feature (sat < 85%
Key diagnostic feature ... FiO2 Severity of symptoms ... CHF, pneumonia, ... Concentrations #Signs ... #Symptoms
Prader-Willi Syndrome: Pathogenesis and clinical findings
 • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome Signs ... /Symptoms/Complications ... Incr Skeletal fractures ... pathophysiology #peds
Childhood Immunization Schedule: Why we immunize
 • Diphtheria Toxin -> URT inflammation causes pseudomembrane with hardened
hemorrhagic rash; symptoms ... of shock • Mumps ... , pharyngitis; pneumonia ... non-specific viral symptoms ... #Immunization #peds
Acute Otitis Media: Pathogenesis and Clinical Findings (in Children)
Upper Respiratory Tract Infection: 
 - Bacterial: Streptococcus
Streptococcus pneumoniae ... 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 ... endocrinology #peds