34 results
Clinical Algorithm for Emergency Department Evaluation and Management of UTI in Febrile Infants and Young Children

Urinary
Clinical Algorithm ... do not replace clinical ... UTI #Algorithm #Diagnosis ... #Peds #UrinaryTract ... #Pediatrics #Fever
Clinical features of shock from dehydration in an infant

Decreased level of consciousness 
Sunken fontanelle 
Dry mucous
Clinical features ... dehydration in an infant ... #PhysicalExam #Signs ... #Dehydration #Peds ... #Pediatrics
Scarf Sign (Normal) on Physical Exam

The scarf sign is used to assess developmental age and muscle
Scarf Sign (Normal ... The infant's arm ... #clinical #video ... hypotonia #hypotonic #peds ... #pediatrics #tone
Kernig's Sign in Meningitis

Kernig's sign is present if the patient, in the supine position with the
Kernig's Sign in ... this video, the infant ... #Meningitis #Clinical ... #PhysicalExam #Pediatrics ... #Peds #neurology
Prader-Willi Syndrome: Pathogenesis and clinical findings
 • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical ... Prader-Willi Syndrome Signs ... delayed puberty -> Infertility ... pathophysiology #peds ... #pediatrics
Standardized Physical Abuse Guideline
<6 months of age
 • Social work consult
 • Skeletal survey
 • Head
• Troponin for infants ... AST or ALT> 80, signs ... Guidelines #Workup #Peds ... #Pediatrics #Diagnosis
The infant with tachypnea or wheeze - Clinical Conditions to Consider
 - Bronchiolitis 
 - Pneumonia
The infant with ... tachypnea or wheeze - Clinical ... Other causes #Diagnosis ... #Peds #Pediatrics ... #Infant #Tachypnea
perioral cyanosis- A blue color around the lips and philtrum is a relatively common finding shortly
The skin in this infant ... #clinical #photo ... #peds #pediatrics
Epiglottitis - Swollen inflamed epiglottis 
Clinical (Rapid onset) 
 • Fever 
 • Sore throat
inflamed epiglottis Clinical ... #Epiglottitis #Signs ... #Causes #Diagnosis ... #Differential #Peds ... #Pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... deficiencies present in infants ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics