22 results
Causes of Sudden Unexpected Death in Infancy (SUDI) - Differential Diagnosis Algorithm
Congenital Anomaly / Disorder:
 •
Unexpected Death in Infancy ... (SUDI) - Differential ... Death Syndrome ... #Infant #Differential ... Algorithm #Causes #Peds
Causes of Pediatric Spells - Differential Diagnosis Algorithm
Neonates and Infant Spells:
 • Benign Sleep Myoclonus
 •
Pediatric Spells - Differential ... Neonates and Infant ... Colic • Sandifer Syndrome ... Older Infants ... Algorithm #Causes #Peds
Causes of Pediatric Seizures - Differential Diagnosis Algorithm
Infantile:
 • Benign Focal Epilepsy of Infancy
 • West
Pediatric Seizures - Differential ... Focal Epilepsy of Infancy ... Older Infants ... Seizures #Epilepsy #Differential ... Algorithm #Causes #Peds
Causes of Unprovoked Pediatric Seizures -  Epilepsy Syndromes - Differential Diagnosis Algorithm 
Infantile:
 • Benign
- Differential ... Focal Epilepsy of Infancy ... • West Syndrome ... Unprovoked #Seizures #Differential ... Algorithm #Causes #Peds
Preterm Infant Complications - Differential Diagnosis
Respiratory:
 • Transient Tachypnea of the Newborn (TTN)
 • Respiratory Distress
Preterm Infant Complications ... - Differential ... Respiratory Distress Syndrome ... Preterm #Premature #Infant ... Diagnosis #Causes #Peds
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 ... #Hypotonic #Infant ... Algorithm #Causes #Peds
Causes of Apparent Life Threatening Event (ALTE) - Differential Diagnosis Algorithm
Cardiac:
 • Congenital Heart Disease
 •
Event (ALTE) - Differential ... Metabolism • Reye's Syndrome ... Breathing • Apnea of Infancy ... Event #ALTE #BRUE #Differential ... Algorithm #Causes #Peds
Erythematous Rashes - THE ALGORITHMIC APPROACH

Characterized by diffuse redness of the skin due to
capillary congestion, erythematous
(SSS) in infants ... Nikolsky sign, the differential ... and toxic shock syndrome ... #Diagnosis #Dermatology ... Febrile #Fever #Differential
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
deficiencies present in infants ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Schematic representation of the major sources of ammonia production and its excretory pathway (GI = gastrointestinal,
rare): - Reye syndrome ... (Peds) - Primary ... deficiency #Ammonia #Pathophysiology ... Hyperammonemia #Differential