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diagnosis differential algorithm clinical infant 21hydroxylasedeficiency 21ohd acrocyanosis anatomy childhood circulation complications congenital cyanosis depressed dermatology diagram endocrinology examination fallot
Causes of Respiratory Distress in the Newborn - Differential Diagnosis Algorithm Premature Newborn - Normal CXR:
Causes of Respiratory ... Respiratory Distress Syndrome ... Respiratory Distress Syndrome ... Diagnosis #Algorithm #Causes ... #Peds #Pediatrics
Causes of Depressed / Lethargic Newborn - Differential Diagnosis Algorithm Maternal Related: • Drugs (Ex. SSRI) •
Causes of Depressed ... / Lethargic Newborn ... Respiratory Distress Syndrome ... Diagnosis #Algorithm #Causes ... #Peds #Pediatrics
Tetralogy of Fallot Summary • Anatomy • Incidence • Pathophysiology • Presentation • Common Variants •
• Incidence • Pathophysiology ... Associated Genetic Syndromes ... diagnosis #management #cardiology ... #peds #pediatrics
Staphylococcal Scalded Skin Syndrome (SSSS) A 5-year-old girl presents to the ED with a rash that started
Staphylococcal Scalded Skin ... Syndrome (SSSS) ... #Syndrome #SSSS ... #Clinical #Photo ... #Peds #Pediatrics
perioral cyanosis- A blue color around the lips and philtrum is a relatively common finding shortly
The skin in this ... #clinical #photo ... #peds #pediatrics ... #newborn #perioral
Preterm Infant Complications - Differential Diagnosis Respiratory: • Transient Tachypnea of the Newborn (TTN) • Respiratory Distress
Tachypnea of the Newborn ... Respiratory Distress Syndrome ... Differential #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 ... Other Congenital Syndromes ... Infant #Floppy #Newborn ... #Peds #Pediatrics
Childhood Immunization Schedule: Why we immunize • Diphtheria Toxin -> URT inflammation causes pseudomembrane with hardened
URT inflammation causes ... that persists as skin ... > Inflammation causes ... #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 ... cold & mottled skin ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds ... #pediatrics
Newborn Infant - Routine Examination Birthweight, gestational age and birthweight percentile are noted. General observation Of the baby's
Newborn Infant - ... with pigmented skin ... #Newborn #Infant ... #Examination #Peds ... #Pediatrics #Diagnosis
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