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diagnosis management pediatrics signs genetics cardiology comparison criticalcare differential endocrinology etoh iem metabolism neonatology nicu psychiatry syndrome treatment 21hydroxylasedeficiency 21ohd
A schema of the pathophysiology of the inborn errors of metabolism, excluding complex storage diseases. Helps
the lab values table ... #Diagnosis #Algorithm ... #Neonatology #Peds ... #Pediatrics #Table ... #IEM #NICU #InbornErrors
Lab patterns seen in Inborn Errors of Metabolism A table of lab values compiled from UpToDate and
Metabolism A table ... metabolicemergency-pathophysiology-differential-pediatrics-metabolism-algorithm-diagnosis ... #InbornErrors ... #Neonatology #Peds ... #Pediatrics #Table
Childhood Immunization Schedule: Why we immunize • Diphtheria Toxin -> URT inflammation causes pseudomembrane with hardened
neurons -> Trismus, tachycardia ... hemorrhagic rash; symptoms ... non-specific viral symptoms ... #Immunization #peds ... #pediatrics #pathophysiology
Mechanical Bowel Obstruction and Ileus - Pathogenesis and Clinical Findings Ileus: Functional bowel "blockage", no peristalsis Mechanical Obstruction:
Pathogenesis and Clinical ... pain and related symptoms ... low JVP, resting tachycardia ... percussion • Nausea ... obstruction #sbo #ileus #pathophysiology
Alcohol Use Disorder: Pathogenesis and Clinical Findings • Tolerance (reduced sensitivity to effects of EtOH) •
Pathogenesis and Clinical ... • Withdrawal symptoms ... - Sweating, tachycardia ... , nausea/vomiting ... AlcoholUseDisorder #EtOH #Pathophysiology
Cold Urticaria Prevalence - 0.05% in the population Disease onset - Mostly 2nd to 4th decades of life Causes
decades of life Causes ... and clinical associations ... and duration of symptoms ... pain, diarrhea, Tachycardia ... rheumatology #comparison #table
Diabetic Ketoacidosis (DKA) - Pathogenesis and Clinical Findings • Note: in DKA, body K+ is lost
Pathogenesis and Clinical ... out of cells may cause ... Signs/Symptoms/Complications ... hypotension/postural tachycardia ... DiabeticKetoacidosis #DKA #pathophysiology
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 ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds
Sarcoidosis - Diagnosis and Management Summary Epidemiology 1) High incidence in Scandinavian countries (11-24 cases per 100,000 individuals
survival is 93-95% Pathophysiology ... renal failure Clinical ... Features: • Many symptoms ... patients have no symptoms ... Self-limiting, chronic but stable
TRALI vs TACO - Transfusion Reactions TRALI: • Epidemiology: 0.1% of transfused patientsl • Risk factors: Critical
Risk factors: Critical ... blood donor • Pathophysiology ... without other cause ... ARDS to explain symptoms ... diagnosis #comparison #table
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