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diagnosis peds differential genetics neonatology nicu birth causes growthcharts iem inbornerrors length management metabolism percentiles weight 21hydroxylasedeficiency 21ohd agraphia alexia
Causes of Pediatric Spells - Differential Diagnosis Algorithm Neonates and Infant Spells: • Benign Sleep Myoclonus •
Causes of Pediatric ... Differential Diagnosis Algorithm ... Neonates and Infant ... Syndrome Older Infants ... Torticollis • Night
Lab patterns seen in Inborn Errors of Metabolism A table of lab values compiled from UpToDate and
Lab patterns seen ... Metabolism A table ... metabolicemergency-pathophysiology-differential-pediatrics-metabolism-algorithm-diagnosis ... #Table #NICU #Genetics ... IEM #Laboratory #Patterns
Causes of Pediatric Seizures - Differential Diagnosis Algorithm Infantile: • Benign Focal Epilepsy of Infancy • West
Causes of Pediatric ... Differential Diagnosis Algorithm ... Torticollis • Night ... Differential #Diagnosis #Algorithm ... #Causes #Peds #Pediatrics
A schema of the pathophysiology of the inborn errors of metabolism, excluding complex storage diseases. Helps
schema of the pathophysiology ... the lab values table ... , UpToDate #Pediatrics ... #Diagnosis #Algorithm ... #Table #IEM #NICU
gestational diabetes algorithm #Infant #Diabetic #Mother #Pediatrics #Neonatology #IDM #NICU #OBGYN #Diagnosis #Pathophysiology #Maternal #Complications #Peds #Newborn
gestational diabetes algorithm ... #Infant #Diabetic ... #Mother #Pediatrics ... OBGYN #Diagnosis #Pathophysiology
Pediatric SVT - Management Algorithm Identify SVT: • HR not variable • Abrupt rate changes • Infants:
Pediatric SVT - ... Management Algorithm ... rate changes • Infants ... Monitors, Pads AP Stable ... #peds #Pediatric
Alexia Without Agraphia Alexia without agraphia is a disconnection syndrome where patients cannot read but can write.
and may have a right ... hemianopsia or right ... Pathophysiology: ... PCA Infarct (most ... neurology #diagnosis #pathophysiology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
deficiencies present in infants ... decr feeding, weight ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds #pediatrics
Lymphomas and Lymphoproliferative Disorders - Differential Diagnosis Algorithm Hodgkin Lymphoma ~40% - Characteristic For Reed-Sternberg (RS) Cells
Differential Diagnosis Algorithm ... involvement, irregular pattern ... age range • High ... Classification #pathophysiology ... #differential #algorithm
This chart shows the patterns of height (length) and weight for children from birth to 36
chart shows the patterns ... of height (length ... Diagnosis #Peds #Pediatrics ... #Males #Birth #Infant ... #Weight #Height
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