21 results
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
Causes of Hypotonic Infant (Floppy Newborn) - Differential Diagnosis Algorithm
Central Nervous System - Decreased LOC, Axial
Causes of Hypotonic ... Infant (Floppy Newborn ... Syndromes - Spinal ... Infant #Floppy #Newborn ... #Peds #Pediatrics
Prader-Willi Syndrome: Pathogenesis and clinical findings
 • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome ... Pathogenesis and clinical ... Signs/Symptoms ... #genetics #pathophysiology ... #peds #pediatrics
Childhood Immunization Schedule: Why we immunize
 • Diphtheria Toxin -> URT inflammation causes pseudomembrane with hardened
hemorrhagic rash; symptoms ... organ ischemia -> Congenital ... non-specific viral symptoms ... #Immunization #peds ... #pediatrics #pathophysiology
Alzheimer’s Disease: Pathogenesis and Clinical Findings
Risk factor for Late Onset Alzheimer's (99% of cases):
 - Increasing
Pathogenesis and Clinical ... mutations - Down syndrome ... chromosome 21) Signs / Symptoms ... AlzheimersDisease #Dementia #pathophysiology ... diagnosis #signs #symptoms
Fat Embolism Syndrome
Trauma to the long bone or pelvis accounts for —9096 of cases. The diagnosis
Fat Embolism Syndrome ... accounts for —9096 of cases ... Pathophysiology ... FES is a clinical ... Diagnosis #Signs #Symptoms
Inherited Non-hemolytic Disorders of Hyperbilirubinemia 

== Disorders of Conjugation ==
Gilbert Syndrome:
 • 5-10% of the population
as jaundice on clinical ... examination; nonspecific symptoms ... Newborn: associated ... and stress may cause ... Hyperbilirubinemia #Inherited #Congenital
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... enzyme 21-OHase causes ... also known as "congenital ... Signs/Symptoms/Complications ... endocrinology #peds
Refeeding Syndrome Overview

What Is It?
	• Electrolyte/fluid shifts caused by initiation of nutrition in severely malnourished patient.
Electrolyte/fluid shifts caused ... changes and may cause ... severe clinical ... overload) Other Symptoms ... Differential #Diagnosis #Pathophysiology