18 results
diagnosis management peds causes syndrome differential endocrinology nephrology hematology iem inbornerrors metabolism neonatology nicu table 21hydroxylasedeficiency 21ohd anxiety apml asthma
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
of congenital adrenal ... #CAH #algorithm ... #causes #pediatrics ... diagnosis #comparison #treatment ... #pathophysiology
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 ... cardiology #peds #pediatrics ... #treatment
Pathogenesis of Anxiety Disorders Anxiety Disorders: A maladaptive emotional state causing fear, worry, and excessive stress, characterized by:
foreboding or apprehension ... reporting rates) • Genetics ... Imbalance and/or abnormal ... Anxiety #Disorders #Pathophysiology
Causes of Growth Restriction - Small for Gestational Age - Differential Diagnosis Algorithm Maternal • Chronic Maternal
Differential Diagnosis Algorithm ... Sickle Cell) • Renal ... Chromosomal Anomaly • Genetic ... Placenta Previa • Abnormal ... Causes #Obstetrics #Pediatrics
Short Stature - Differential Diagnosis Algorithm Normal Variant, Normal Puberty Onset (BA = CA) • Familial Short
Differential Diagnosis Algorithm ... • Congenital Adrenal ... Panhypopituitarism Treatment ... Differential #Diagnosis #Algorithm ... endocrinology #causes #pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
21-OHD in the adrenal ... as "congenital adrenal ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
BRASH Syndrome B - Bradycardia R - Renal failure A - AV nodal blockade S - Shock H - Hyperkalemia Typical ECG
Bradycardia R - Renal ... hyperkalemia) BRASH Treatment ... • Aggressive treatment ... balanced fluids" > normal ... diagnosis #management #pathophysiology
Algorithm for the Treatment of Membranous Lupus Nephritis Sub-nephrotic-range proteinuria (<3.5g/d, normal serum albumin) and Preserved kidney
Algorithm for the ... Treatment of Membranous ... proteinuria (<3.5g/d, normal ... Lupus #Nephritis #Algorithm ... #Treatment #management
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