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physicalexam diagnosis video differential neurology newborn primitive infant 21hydroxylasedeficiency 21ohd alte brudzinskis brue deeptendon endocrinology event examination failuretothrive floppy ftt
Causes of Pediatric Wheezing - Differential Diagnosis Algorithm CXR Abnormal: • Pulmonary Sequestration • Congenital Adenoid Cystic
Causes of Pediatric ... Differential Diagnosis Algorithm ... CXR Abnormal: ... Aspiration • GE Reflux ... #Causes #Peds #
Causes of Apparent Life Threatening Event (ALTE) - Differential Diagnosis Algorithm Cardiac: • Congenital Heart Disease •
Causes of Apparent ... Differential Diagnosis Algorithm ... Gastroesophageal Reflux ... #Causes #Peds # ... Pediatrics
Moro Reflex on Newborn Physical Exam The Moro reflex is obtained by holding the baby’s head and
Moro Reflex on Newborn ... is obtained by holding ... #Moro #Reflex #Peds ... #Pediatrics #Clinical ... Video #Neurology #Normal
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 Causes of Hypotonic Infant (Floppy Newborn) - Differential Diagnosis Algorithm Central Nervous System - Decreased LOC, Axial
Causes of Hypotonic ... Strength, Normal ... Reflexes - Brain ... #Causes #Peds # ... Pediatrics
Causes of Failure to Thrive - Differential Diagnosis Algorithm Adequate Calorie Consumption - Increased Losses:
Causes of Failure ... Gastroesophageal Reflux ... Illness: • Oral ... #Causes #Peds # ... Pediatrics
Landau's Reaction (Reflex) on Physical Exam Landau's reaction is investigated holding the baby firmly under the
Landau's Reaction (Reflex ... is investigated holding ... #PhysicalExam #clinical ... video #Neurology #Peds ... #Pediatrics #Normal
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 Galant Reflex on Physical Exam The Galant reflex is present at birth and remains until the 2nd
Galant Reflex on ... persistent in cases ... #PhysicalExam #clinical ... video #Neurology #Peds ... #Pediatrics #Normal
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 Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski) Brudzinski's sign is characterized
Passive neck flexion causes ... While the pathophysiology ... an involuntary reflex ... #PhysicalExam #Pediatrics ... #Peds
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 21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... mutation in CYP21A2 coding ... enzyme 21-OHase causes ... endocrinology #peds ... #pediatrics
Newborn Infant - Routine Examination Birthweight, gestational age and birthweight percentile are noted. General observation Of the baby's
checked for red reflex ... This reflex is not ... the heart, the normal ... #Examination #Peds ... #Pediatrics #Diagnosis
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