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peds diagnosis table neonatology nicu patientinfo background chestxray comparison ct differential doses iem imaging inbornerrors management metabolism nuclear radiation radiology
A schema of the pathophysiology of the inborn errors of metabolism, excluding complex storage diseases. Helps
schema of the pathophysiology ... , UpToDate #Pediatrics ... MetabolicEmergency #Genetics ... #Pathophysiology ... #Diagnosis #Algorithm
Lab patterns seen in Inborn Errors of Metabolism A table of lab values compiled from UpToDate and
from UpToDate and Pediatrics ... metabolicemergency-pathophysiology-differential-pediatrics-metabolism-algorithm-diagnosis ... Neonatology #Peds #Pediatrics ... #Table #NICU #Genetics
Tetralogy of Fallot Summary • Anatomy • Incidence • Pathophysiology • Presentation • Common Variants •
• Incidence • Pathophysiology ... • Associated Genetic ... diagnosis #management #cardiology ... #peds #pediatrics
Estimated Medical Radiation Doses for 5 Year-Old Child 3-view ankle 0.0015 mSv 1/14th CXRs 2-view chest 0.02 mSv 1 CXRs Anteroposterior and lateral
0.0015 mSv 1/14th CXRs ... American Academy of Pediatrics ... #PatientInfo #Radiology ... #Table #Risks #Testing ... #Study #Peds #Pediatrics
gestational diabetes algorithm #Infant #Diabetic #Mother #Pediatrics #Neonatology #IDM #NICU #OBGYN #Diagnosis #Pathophysiology #Maternal #Complications #Peds #Newborn
gestational diabetes algorithm ... Diabetic #Mother #Pediatrics ... OBGYN #Diagnosis #Pathophysiology ... Antenatal #Visits #Testing
Diagnostic algorithm for a child or adolescent with suspected pulmonary hypertension. CHD, congenital heart disease; CPET,
Diagnostic algorithm ... cardiopulmonary exercise testing ... hypertension; CXR ... Diagnosis #Peds #Pediatrics ... Hypertension #Workup #Algorithm
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
, sleep apnea, cor ... PraderWilli #Syndrome #genetics ... #pathophysiology ... #peds #pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
glands • Salt wasting ... infants with "salt wasting ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
How much radiation is used in paediatric radiology examinations compared to other exposures? Estimated dose - Days
radiation is used in paediatric ... radiology examinations ... Imaging #ChestXRay #CXR ... #Table #Risks #Testing ... #Study #Peds #Pediatrics
Pragmatic diagnostic algorithm for hypokalemia. ***Typical presentations: • Vomiting: urine Na/Cl > 1.6, low urine
Pragmatic diagnostic algorithm ... K/creatinine (Cr ... confirmed via genetic ... testing *If hypokalemia ... #differential #algorithm
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