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

Urinary
Clinical Algorithm ... American Academy of Pediatrics ... interest of advancing pediatric ... #Peds #UrinaryTract ... #Pediatrics #Fever
Clinical features of shock from dehydration in an infant

Decreased level of consciousness 
Sunken fontanelle 
Dry mucous
Clinical features ... membranes Eyes sunken and ... #PhysicalExam #Signs ... #Symptoms #Shock ... #Peds #Pediatrics
Scarf Sign (Normal) on Physical Exam

The scarf sign is used to assess developmental age and muscle
Scarf Sign (Normal ... developmental age and ... #clinical #video ... hypotonia #hypotonic #peds ... #pediatrics #tone
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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
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Prader-Willi Syndrome: Pathogenesis and clinical findings
 • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome Signs ... /Symptoms/Complications ... PraderWilli #Syndrome #genetics ... pathophysiology #peds ... #pediatrics
The infant with tachypnea or wheeze - Clinical Conditions to Consider
 - Bronchiolitis 
 - Pneumonia
The infant with ... tachypnea or wheeze - Clinical ... following viral lower ... #Diagnosis #Peds ... #Pediatrics #Infant
Algorithm for the Evaluation and Management of Suspected Congenital Heart Disease in Neonates

Neonates with undiagnosed congenital
Management of Suspected ... with nonspecific symptoms ... Algorithm #Evaluation #Management ... Neonates #Neonatal #Peds ... #Pediatrics #Cardiology
Bronchiolitis
Bronchiolitis is a viral inflamation of the bronchioles and the commonest LRTI in under 1s'. It's
Diagnosis - Coryzal symptoms ... REMEMBER - infants ... Bronchiolitis #pediatrics ... #diagnosis #management ... #peds #treatment
Clinical Features and Complications of Measles

Rash:
Spreads downwards, from behind the ears to the whole Of the
Clinical Features ... and Complications ... Kopliks KoplikSpots #Peds ... #Pediatrics #Timeline ... #Signs #Symptoms
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Clinical Findings ... Signs/Symptoms/Complications ... pathophysiology #genetics ... endocrinology #peds ... #pediatrics