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differential infant fever management pathophysiology physicalexam seizures symptoms 21hydroxylasedeficiency 21ohd cardiology chf classification cries criticalcare dementia dims disease endocrinology epiglottitis
The Febrile Child - some diagnostic clues to evaluating the febrile child. #Febrile #Fever #Evaluation #Assessment #Signs
- some diagnostic ... clues to evaluating ... #Evaluation #Assessment ... #Signs #Symptoms ... #Peds #Pediatrics
Causes of Pediatric Stridor - Differential Diagnosis Algorithm Present Since Infancy with No Respiratory Distress: • Laryngomalacia Present
Causes of Pediatric ... Algorithm Present ... Acute Onset Febrile ... #Algorithm #Causes ... #Peds #Pediatrics
Clinical Algorithm for Emergency Department Evaluation and Management of UTI in Febrile Infants and Young Children Urinary
Clinical Algorithm ... Management of UTI in Febrile ... #Diagnosis #Management ... #Febrile #Infant ... #Peds #UrinaryTract
Epiglottitis - Swollen inflamed epiglottis Clinical (Rapid onset) • Fever • Sore throat
inflamed epiglottis Clinical ... #Epiglottitis #Signs ... #Causes #Diagnosis ... #Differential #Peds ... #Pediatrics
Causes of Pediatric Seizures - Differential Diagnosis Algorithm Infantile: • Benign Focal Epilepsy of Infancy • West
Causes of Pediatric ... Algorithm Infantile ... Infection: • Febrile ... #Algorithm #Causes ... #Peds #Pediatrics
Causes of Provoked Pediatric Seizures - Differential Diagnosis Algorithm - "DIMS" Mnemonic Drugs: • Drug overdose •
Causes of Provoked ... Pediatric Seizures ... Infection: • Febrile ... #Algorithm #Causes ... #Peds #Pediatrics
The infant with tachypnea or wheeze - Clinical Conditions to Consider - Bronchiolitis - Pneumonia
tachypnea or wheeze - Clinical ... disorder - Other causes ... #Diagnosis #Peds ... #Pediatrics #Infant ... #Differential #Assessment
CRIES is a 10-point scale, using a physiologic basis similar to APGAR: Crying; Requires increased oxygen
Increased vital signs ... in the ED, the clinician ... #Diagnosis #Peds ... #Pediatrics #PainScale ... PostOperative #Assessment
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... enzyme 21-OHase causes ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics
Major neurocognitive disorders (MNCD): Diagnosis and workup 1) Clinical diagnosis Cognitive impairment + loss of autonomy 2)
workup 1) Clinical ... neuropsychological assessment ... Alzheimer - 1st cause ... (parkinsonian signs ... #Geriatrics #Workup
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