16 results
Summary of problems of Very Low Birthweight Infants

#Premature #Low #Birthweight #Peds #Pediatrics #Problems #Signs #Symptoms #Presentation
Low Birthweight Infants ... #Birthweight #Peds ... #Pediatrics #Problems ... #Signs #Symptoms
Tetralogy of Fallot 

1. Right ventricular outflow tract obstruction 

2. Right ventricular hypertrophy 

3. Ventricular septal
Ventricular septal defect ... Tetralogy #Fallot #Peds ... #Pediatrics #Cardiology ... #Signs #Symptoms
Clinical features of shock from dehydration in an infant

Decreased level of consciousness 
Sunken fontanelle 
Dry mucous
dehydration in an infant ... #PhysicalExam #Signs ... #Symptoms #Shock ... #Infant #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
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Pediatric SVT - Management Algorithm
Identify SVT:
 • HR not variable
 • Abrupt rate changes
 • Infants:
Pediatric SVT - ... rate changes • Infants ... Signs of shock or ... #Algorithm #peds ... #Pediatric #treatment
Kernig's Sign in Meningitis

Kernig's sign is present if the patient, in the supine position with the
In this video, the ... infant cries as ... Meningitis #Clinical #Video ... #PhysicalExam #Pediatrics ... #Peds #neurology
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Kawasaki Disease (Mucocutaneous Lymph Node Syndrome) 
An rare systemic acute febrile vasculitic syndrome. Aetiology unknown. 
Affects
Affects children ... Disease #Features #Signs ... #Symptoms #Diagnosis ... #Peds #Pediatrics
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
PECARN Head CT Decision Aid

The Head CT Choice decision aid was developed in Rochester, Minnesota. Full
observation, and signs ... and symptoms that ... (Figure 2) #Management ... #PatientInfo #Peds ... #Pediatrics #DecisionAid
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
deficiencies present in infants ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics