11 results
diagnosis video genetics newborn pathophysiology tone 21hydroxylasedeficiency 21ohd adult algorithm breathing dehydration distress endocrinology evaluation examination febrile fever hand hypotonia
Signs and Symptoms of Respiratory Distress Through the Years. #signs #symptoms #diagnosis #differential #neonatal #pediatrics #adult
Signs and Symptoms ... #signs #symptoms ... #neonatal #pediatrics ... #adult #peds #pulmonary ... #causes
Causes of Pediatric Stridor - Differential Diagnosis Algorithm Present Since Infancy with No Respiratory Distress: • Laryngomalacia Present
Causes of Pediatric ... Stridor - Differential ... with Respiratory ... #Peds #Pediatrics ... #Pulmonary
The Febrile Child - some diagnostic clues to evaluating the febrile child. #Febrile #Fever #Evaluation #Assessment #Signs
Fever #Evaluation #Assessment ... #Signs #Symptoms ... #PhysicalExam # ... Diagnosis #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 ... #Assessment #Wheezing
Scarf Sign (Normal) on Physical Exam The scarf sign is used to assess developmental age and muscle
muscle tone in neonates ... #Scarf #Sign #PhysicalExam ... #clinical #video ... hypotonia #hypotonic #peds ... #pediatrics #tone
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 Clinical features of shock from dehydration in an infant Decreased level of consciousness Sunken fontanelle Dry mucous
Clinical features ... Extremities #PhysicalExam ... #Signs #Symptoms ... #Dehydration #Peds ... #Pediatrics
Paradoxical Breathing on Physical Exam Paradoxical breathing is often a sign of breathing problems. It causes the
breathing is often a sign ... It causes the chest ... #respiratory #clinical ... #video #pulmonary ... #peds #pediatrics
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 Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical ... /Symptoms/Complications ... Poor suckling -> Neonatal ... pathophysiology #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 ... enzyme 21-OHase causes ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics
Newborn Infant - Routine Examination Birthweight, gestational age and birthweight percentile are noted. General observation Of the baby's
always needs urgent assessment ... of respiratory ... #PhysicalExam # ... Examination #Peds ... #Pediatrics #Diagnosis
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