11 results
physicalexam clinical newborn diagnosis meningitis pathophysiology primitive tone 21hydroxylasedeficiency 21ohd anomalous babinski breathing brudzinskis cardiology endocrinology examination hand hypotonia hypotonic
Scarf Sign (Normal) on Physical Exam The scarf sign is used to assess developmental age and muscle
Scarf Sign (Normal ... Exam The scarf sign ... #Scarf #Sign #PhysicalExam ... #clinical #video ... #pediatrics #tone
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 Kernig's Sign in Meningitis Kernig's sign is present if the patient, in the supine position with the
Kernig's Sign in ... Meningitis Kernig's sign ... infant cries as ... Prakash #Kernigs #Sign ... #PhysicalExam #Pediatrics
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 Paradoxical Breathing on Physical Exam Paradoxical breathing is often a sign of breathing problems. It causes the
breathing is often a sign ... 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
Prader-Willi Syndrome Signs ... pulmonale #PraderWilli ... #Syndrome #genetics ... pathophysiology #peds ... #pediatrics
Total Anomalous Pulmonary Venous Return (TAPVR) • Introduction • Classification • Pathophysiology of TAPVR • Presentation
Total Anomalous Pulmonary ... Classic “snowman sign ... Total #Anomalous #Pulmonary ... diagnosis #management #cardiology ... #peds #pediatrics
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski) Brudzinski's sign is characterized
Brudzinski’s Sign ... Brudzinski's sign ... an involuntary reflex ... #PhysicalExam #Pediatrics ... #Peds
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 Plantar Reflex on Newborn Physical Exam The normal response to stroking the lateral aspect of the
Plantar Reflex on ... toes or “Babinski sign ... normal in the infant ... PhysicalExam #clinical #video ... #peds #pediatrics
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 Primitive Suck, Rooting Reflex on Newborn Physical Exam The normal response to stroking the lateral aspect
Suck, Rooting Reflex ... toes or “Babinski sign ... normal in the infant ... PhysicalExam #clinical #video ... #peds #pediatrics
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 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 ... pathophysiology #genetics ... endocrinology #peds ... #pediatrics
Newborn Infant - Routine Examination Birthweight, gestational age and birthweight percentile are noted. General observation Of the baby's
is also a late sign ... paediatrician or geneticist ... are observed for signs ... #Examination #Peds ... #Pediatrics #Diagnosis
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