14 results
Signs and Symptoms of Respiratory Distress Through the Years. 

#signs #symptoms #diagnosis #differential #neonatal #pediatrics #adult
Signs and Symptoms ... #signs #symptoms ... #differential #neonatal ... #pediatrics #adult ... #peds #pulmonary
Algorithm for the Evaluation and Management of Suspected Congenital Heart Disease in Neonates

Neonates with undiagnosed congenital
Heart Disease in Neonates ... Neonates with ... with nonspecific symptoms ... #Neonatal #Peds ... #Pediatrics #Cardiology
Scarf Sign (Normal) on Physical Exam

The scarf sign is used to assess developmental age and muscle
Scarf Sign (Normal ... muscle tone in neonates ... #clinical #video ... hypotonia #hypotonic #peds ... #pediatrics #tone
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
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
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
Tetralogy of Fallot 

1. Right ventricular outflow tract obstruction 

2. Right ventricular hypertrophy 

3. Ventricular septal
Tetralogy #Fallot #Peds ... #Pediatrics #Cardiology ... #Signs #Symptoms
Prader-Willi Syndrome: Pathogenesis and clinical findings
 • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome Signs ... /Symptoms/Complications ... Poor suckling -> Neonatal ... pathophysiology #peds ... #pediatrics
Neonatal Resuscitation - Preparation and Overview
Preparation:
 - All health professionals dealing with newborn infants should be
Neonatal Resuscitation ... not, commence neonatal ... Remove any wet towels ... #Preparation #peds ... #management #pediatrics
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