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diagnosis algorithm epilepsy seizures 21hydroxylasedeficiency 21ohd alte brudzinskis brue clinical complications epilepsies event floppy genetics hypotonic infancy lifethreatening meningitis newborn
Causes of Pediatric Spells - Differential Diagnosis Algorithm Neonates and Infant Spells: • Benign Sleep Myoclonus •
Causes of Pediatric ... Spells - Differential ... Colic • Sandifer Syndrome ... Older Infants ... #Peds #Pediatrics
Causes of Sudden Unexpected Death in Infancy (SUDI) - Differential Diagnosis Algorithm Congenital Anomaly / Disorder: •
Causes of Sudden ... (SUDI) - Differential ... Death Syndrome ... #Infant #Differential ... #Peds #Pediatrics
Causes of Unprovoked Pediatric Seizures - Epilepsy Syndromes - Differential Diagnosis Algorithm Infantile: • Benign
Causes of Unprovoked ... Pediatric Seizures ... - Differential ... Focal Epilepsy of Infancy ... #Peds #Pediatrics
Causes of Pediatric Seizures - Differential Diagnosis Algorithm Infantile: • Benign Focal Epilepsy of Infancy • West
Causes of Pediatric ... Seizures - Differential ... Seizures #Epilepsy #Differential ... Diagnosis #Algorithm #Causes ... #Peds #Pediatrics
Preterm Infant Complications - Differential Diagnosis Respiratory: • Transient Tachypnea of the Newborn (TTN) • Respiratory Distress
- Differential ... Respiratory Distress Syndrome ... Enterocolitis (NEC ... #Diagnosis #Causes ... #Peds #Pediatrics
Causes of Hypotonic Infant (Floppy Newborn) - Differential Diagnosis Algorithm Central Nervous System - Decreased LOC, Axial
Causes of Hypotonic ... Infant (Floppy ... Newborn) - Differential ... Other Congenital Syndromes ... #Peds #Pediatrics
Causes of Apparent Life Threatening Event (ALTE) - Differential Diagnosis Algorithm Cardiac: • Congenital Heart Disease •
Causes of Apparent ... Event (ALTE) - Differential ... Metabolism • Reye's Syndrome ... Breathing • Apnea of Infancy ... #Peds #Pediatrics
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski) Brudzinski's sign is characterized
causes spinal cord ... While the pathophysiology ... Video by Dr. ... #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
enzyme 21-OHase causes ... deficiencies present in infants ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
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