12 results
Hypocalcemia - Differential Diagnosis Algorithm - Low and High PTH
LOW PTH - Hypoparathyroid
 - Congenital (Pediatric)
Hypocalcemia - Differential ... Diagnosis Algorithm ... - Congenital (Pediatric ... bypass • Liver ... #PTH #endocrinology
BRUE (Brief Resolved Unexplained Event) Algorithm

ALTE (Apparent Life Threatening Event) is out, replaced with a new
Unexplained Event) Algorithm ... ALTE (Apparent ... Life Threatening ... Management #Peds #Pedatrics ... #ALTE
Hypocalcemia - Diagnosis and Management
PTH Independent (↑ PTH)
 • LOW VIT D
    -
Hypocalcemia - Diagnosis ... - Activation: Liver ... PTH Signaling #Hypocalcemia ... Diagnosis #Management #endocrinology ... #differential #algorithm
Causes of Apparent Life Threatening Event (ALTE) - Differential Diagnosis Algorithm
Cardiac:
 • Congenital Heart Disease
 •
Causes of Apparent Life ... Threatening Event (ALTE ... Differential Diagnosis Algorithm ... LifeThreatening #Event #ALTE ... #Causes #Peds #Pediatrics
Recurrent Polymorphic VT/Torsades de Pointes - Management Algorithm
Drugs that prolong QT interval:
 • Class 1a (quinidine,
Pointes - Management Algorithm ... • Hypocalcemia ... Recurrent TdP First line ... 1 gm/hour • Pediatric ... mcg/min • Pediatric
Apparent Life Threatening Events (ALTE) - Management Algorithm
#Management #Peds #Pedatrics #ALTE #ApparentLifeThreateningEvent #Algorithm #PEMSource
Apparent Life Threatening ... Events (ALTE) - ... Management Algorithm ... Management #Peds #Pedatrics ... #Algorithm #PEMSource
Short Stature - Differential Diagnosis Algorithm
Normal Variant, Normal Puberty Onset (BA = CA)
 • Familial Short
Differential Diagnosis Algorithm ... Short Stature (Late ... Differential #Diagnosis #Algorithm ... #endocrinology ... #causes #pediatrics
Malignant Adrenal Mass - Differential Diagnosis Algorithm
Suggestive of Malignancy: Inhomogenous Density, Delay in CT Contrast Washout
Differential Diagnosis Algorithm ... Hypointense to Liver ... Hypertension +/- Hypokalemia ... Differential #Diagnosis #Algorithm ... #Endocrinology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
, vomiting • Late ... clitoris may look like ... minor fuse to look like ... pathophysiology #genetics #endocrinology ... #peds #pediatrics
Growth Hormone Deficiency - Pediatrics - Testing Algorithm
 - Insulin-Like Growth Factor 1 (IGF-1) with Calculated
Hormone Deficiency - Pediatrics ... - Testing Algorithm ... Hormone #Deficiency #Pediatrics ... #Algorithm #diagnosis ... #endocrinology