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peds diagnosis differential pathophysiology 21hydroxylasedeficiency 21ohd alzheimersdisease dementia ea endocrinology epilepsy esophagealatresia feedingintolerance floppy generalsurgery genetics hypotonia neonate newborn normal
Scarf Sign (Normal) on Physical Exam The scarf sign is used to assess developmental age and muscle
muscle tone in neonates ... The infant's arm ... infant, the elbow ... #PhysicalExam #clinical ... #pediatrics #tone
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 Causes of Pediatric Spells - Differential Diagnosis Algorithm Neonates and Infant Spells: • Benign Sleep Myoclonus •
Causes of Pediatric ... Neonates and Infant ... Syndrome Older Infants ... #Causes #Peds # ... Pediatrics
Causes of Pediatric Seizures - Differential Diagnosis Algorithm Infantile: • Benign Focal Epilepsy of Infancy • West
Causes of Pediatric ... Differential Diagnosis Algorithm ... Sturge-Weber Syndrome Neonates ... #Causes #Peds # ... Pediatrics
Causes of Hypotonic Infant (Floppy Newborn) - Differential Diagnosis Algorithm Central Nervous System - Decreased LOC, Axial
Causes of Hypotonic ... Infant (Floppy ... #Infant #Floppy ... #Causes #Peds # ... Pediatrics
Suggested diagnostic algorithm for neonate with suspected esophageal atresia +/- tracheoesophageal fistula. Image Source: De Virgilio, C.,
Suggested diagnostic algorithm ... for neonate with ... Surgery: A case ... based clinical review ... generalsurgery; #pediatrics
Alzheimer’s Disease: Pathogenesis and Clinical Findings Risk factor for Late Onset Alzheimer's (99% of cases): - Increasing
Pathogenesis and Clinical ... chromosome 21) Signs / Symptoms ... Complications: • Deficit ... pathophysiology #geriatrics ... diagnosis #signs #symptoms
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 ... deficiencies present in infants ... Signs/Symptoms/Complications ... endocrinology #peds #pediatrics
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