19 results
Causes of Sudden Unexpected Death in Infancy (SUDI) - Differential Diagnosis Algorithm
Congenital Anomaly / Disorder:
 •
Causes of Sudden ... - Differential Diagnosis ... Pulmonary Anomaly • Metabolic ... Death Syndrome ... Pediatrics
Causes of Pediatric Seizures - Differential Diagnosis Algorithm
Infantile:
 • Benign Focal Epilepsy of Infancy
 • West
Causes of Pediatric ... - Differential Diagnosis ... Encephalitis Provoked - Metabolic ... #Algorithm #Causes ... #Peds #Pediatrics
Clinical features of shock from dehydration in an infant

Decreased level of consciousness 
Sunken fontanelle 
Dry mucous
Clinical features ... loss Reduced urine ... Extremities #PhysicalExam ... #Signs #Symptoms ... Dehydration #Peds #Pediatrics
Causes of Apparent Life Threatening Event (ALTE) - Differential Diagnosis Algorithm
Cardiac:
 • Congenital Heart Disease
 •
Causes of Apparent ... - Differential Diagnosis ... • Reye's Syndrome ... Breathing • Apnea of Infancy ... #Peds #Pediatrics
Peri-operative Hyperthermia - Guidelines for Crises in Anaesthesia
If prolonged or ≥ 39 C this is a
39 C this is a clinical ... dissipation of metabolic ... maintained fever CAUSES ... devices, especially infants ... Anesthesia #Checklist #Diagnosis
Rhabdomyolysis - Differential Diagnosis Framework and Management Summary

Causes of Rhabdomyolysis:
 • Trauma:
	- Immobilization
	- Crush injury
	- Compartment
- Differential Diagnosis ... Management Summary Causes ... Heat stroke - Metabolic ... Dermatomyositis Clinical ... • Other symptoms
Alzheimer’s Disease: Pathogenesis and Clinical Findings
Risk factor for Late Onset Alzheimer's (99% of cases):
 - Increasing
Pathogenesis and Clinical ... mutations - Down syndrome ... pathophysiology #geriatrics ... #diagnosis #signs ... #symptoms
Refeeding Syndrome Overview

What Is It?
	• Electrolyte/fluid shifts caused by initiation of nutrition in severely malnourished patient.
from hormonal and metabolic ... changes and may cause ... severe clinical ... overload) Other Symptoms ... #Differential #Diagnosis
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 ... deficiencies present in infants ... Signs/Symptoms/Complications ... non-arousable, decr urine
Abnormalities in Rate and Rhythm of Breathing 
Normal 
The respiratory rate is about 14—20 per min
44 per min in infants ... , anxiety, and metabolic ... hyperventilation syndrome—a ... Abnormalities #Abnormal #Diagnosis ... #PhysicalExam