11 results
Causes of Sudden Unexpected Death in Infancy (SUDI) - Differential Diagnosis Algorithm
Congenital Anomaly / Disorder:
 •
Causes of Sudden ... (SUDI) - Differential ... • Metabolic Disorders ... #Infant #Differential ... #Peds #Pediatrics
Causes of Unprovoked Pediatric Seizures -  Epilepsy Syndromes - Differential Diagnosis Algorithm 
Infantile:
 • Benign
Causes of Unprovoked ... Pediatric Seizures ... Focal Epilepsy of Infancy ... West Syndrome • Dravet ... #Peds #Pediatrics
Causes of Pediatric Seizures - Differential Diagnosis Algorithm
Infantile:
 • Benign Focal Epilepsy of Infancy
 • West
Causes of Pediatric ... Seizures - Differential ... West Syndrome • Dravet ... #Epilepsy #Differential ... #Peds #Pediatrics
Causes of Apparent Life Threatening Event (ALTE) - Differential Diagnosis Algorithm
Cardiac:
 • Congenital Heart Disease
 •
Causes of Apparent ... Neurologic: • Seizure ... Neuromuscular • Disorders ... Breathing • Apnea of Infancy ... #Peds #Pediatrics
Causes of Enuresis - Differential Diagnosis Algorithm
Primary Nocturnal Enuresis (Urinary Control Never Achieved)
 • Delayed Maturation
Causes of Enuresis ... - Differential ... Neurogenic Bladder, Seizure ... Disorder) Diurnal ... #Peds #Pediatrics
The infant with tachypnea or wheeze - Clinical Conditions to Consider
 - Bronchiolitis 
 - Pneumonia
neuromuscular disorder ... - Other causes ... #Diagnosis #Peds ... #Pediatrics #Infant ... Tachypnea #Wheeze #Differential
Urine Color - Differential Diagnosis
Red Urine:
 • Medical conditions: bleeding, porphyria, factitious disorder
 • Meds: rifampin,
Urine Color - Differential ... porphyria, factitious disorder ... : • Any cause of ... dyes typically cause ... discoloration #nephrology
Rhabdomyolysis - Differential Diagnosis Framework and Management Summary

Causes of Rhabdomyolysis:
 • Trauma:
	- Immobilization
	- Crush injury
	- Compartment
Rhabdomyolysis - Differential ... Management Summary Causes ... exertion/training - Seizures ... Weakness - Dark urine ... #treatment #nephrology
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 ... non-arousable, decr urine ... endocrinology #peds ... #pediatrics
Causes of Hypotonic Infant (Floppy Newborn) - Differential Diagnosis Algorithm
Central Nervous System - Decreased LOC, Axial
Causes of Hypotonic ... Infant (Floppy ... Newborn) - Differential ... #Hypotonic #Infant ... #Peds #Pediatrics