13 results
pediatrics diagnosis physicalexam newborn clinical video differential management primitive treatment 21hydroxylasedeficiency 21ohd alte babinski brudzinskis brue cord dehydration disease disorders
Clinical features of shock from dehydration in an infant Decreased level of consciousness Sunken fontanelle Dry mucous
dehydration in an infant ... Decreased level ... #PhysicalExam #Signs ... #Dehydration #Peds ... #Pediatrics
Pediatric SVT - Management Algorithm Identify SVT: • HR not variable • Abrupt rate changes • Infants:
Pediatric SVT - ... Management Algorithm ... rate changes • Infants ... Signs of shock or ... #peds #Pediatric
Causes of Hypotonic Infant (Floppy Newborn) - Differential Diagnosis Algorithm Central Nervous System - Decreased LOC, Axial
Infant (Floppy ... Nervous System - Decreased ... Strength, Normal Reflexes ... #Causes #Peds # ... Pediatrics
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski) Brudzinski's sign is characterized
Brudzinski’s Sign ... Passive neck flexion causes ... an involuntary reflex ... #PhysicalExam #Pediatrics ... #Peds
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 Causes of Apparent Life Threatening Event (ALTE) - Differential Diagnosis Algorithm Cardiac: • Congenital Heart Disease •
Causes of Apparent ... Gastroesophageal Reflux ... Breathing • Apnea of Infancy ... #Causes #Peds # ... Pediatrics
Plantar Reflex on Newborn Physical Exam The normal response to stroking the lateral aspect of the
toes or “Babinski sign ... normal in the infant ... Primitive #Babinski #Reflex ... clinical #video #peds ... #pediatrics
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 Primitive Suck, Rooting Reflex on Newborn Physical Exam The normal response to stroking the lateral aspect
toes or “Babinski sign ... normal in the infant ... Rooting #Primitive #Reflex ... clinical #video #peds ... #pediatrics
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 Newborn Infant - Routine Examination Birthweight, gestational age and birthweight percentile are noted. General observation Of the baby's
is also a late sign ... This reflex is not ... are observed for signs ... #Examination #Peds ... #Pediatrics #Diagnosis
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... deficiencies present in infants ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics
Evaluation of suspected incomplete Kawasaki Disease 1. AHA consensus recommendations 2. Infants ≤6 months old on day ≥7
Infants ≤6 months ... lack of tapering, decreased ... clinical and lab signs ... #Diagnosis #Peds ... #Pediatrics #Kawasaki
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