9 results
Causes of Congenital Anomalies - Differential Diagnosis Algorithm
Malformation
 • Embryonic development failure or inadequacy (often multifactorial)
Deformation
Causes of Congenital ... Diagnosis Algorithm ... VACTERL) #Congenital ... #Causes #Peds # ... Pediatrics
Causes of Sudden Unexpected Death in Infancy (SUDI) - Differential Diagnosis Algorithm
Congenital Anomaly / Disorder:
 •
Causes of Sudden ... Differential Diagnosis Algorithm ... Congenital Anomaly ... #Causes #Peds # ... Pediatrics
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
various types of congenital ... #CAH #algorithm ... #causes #pediatrics ... comparison #treatment #Peds ... Endocrinology #Adrenal #pathophysiology
Causes of Pediatric Seizures - Differential Diagnosis Algorithm
Infantile:
 • Benign Focal Epilepsy of Infancy
 • West
Causes of Pediatric ... Differential Diagnosis Algorithm ... • Tumours • Congenital ... #Causes #Peds # ... Pediatrics
Causes of Hypotonic Infant (Floppy Newborn) - Differential Diagnosis Algorithm
Central Nervous System - Decreased LOC, Axial
Causes of Hypotonic ... Infant (Floppy ... Differential Diagnosis Algorithm ... #Causes #Peds # ... Pediatrics
Causes of Cyanosis in the Newborn - Differential Diagnosis Algorithm
Peripheral Only:
 • Poor Perfusion
 • Acrocyanosis
Hemoglobinopathy:
Causes of Cyanosis ... Hemoglobinopathy: • Congenital ... Defect • Total Anomalous ... #Causes #Peds # ... Pediatrics
Causes of Apparent Life Threatening Event (ALTE) - Differential Diagnosis Algorithm
Cardiac:
 • Congenital Heart Disease
 •
Causes of Apparent ... Cardiac: • Congenital ... Breathing • Apnea of Infancy ... #Causes #Peds # ... Pediatrics
Childhood Immunization Schedule: Why we immunize
 • Diphtheria Toxin -> URT inflammation causes pseudomembrane with hardened
URT inflammation causes ... organ ischemia -> Congenital ... anomalies: hearing ... #Immunization #peds ... #pediatrics #pathophysiology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... also known as "congenital ... deficiencies present in infants ... endocrinology #peds ... #pediatrics