19 results
A schema of the pathophysiology of the inborn errors of metabolism, excluding complex storage diseases. Helps
the connections and ... the lab values table ... Diagnosis #Algorithm #Differential ... #Neonatology #Peds ... #Pediatrics #Table
Causes of Pediatric Spells - Differential Diagnosis Algorithm
Neonates and Infant Spells:
 • Benign Sleep Myoclonus
 •
Causes of Pediatric ... Spells - Differential ... Colic • Sandifer Syndrome ... Diagnosis #Algorithm #Causes ... #Peds #Pediatrics
Lab patterns seen in Inborn Errors of Metabolism

A table of lab values compiled from UpToDate and
Metabolism A table ... from UpToDate and ... metabolicemergency-pathophysiology-differential-pediatrics-metabolism-algorithm-diagnosis ... #Neonatology #Peds ... #Pediatrics #Table
Causes of Developmental Delay - Differential Diagnosis Algorithm
Isolated Domain Delay - Reduced Respiratory Drive:
 • Cognitive
Causes of Developmental ... Delay - Differential ... Disorder) Language and ... Landau-Kleffner Syndrome ... #Peds #Pediatrics
Causes of Pediatric Seizures - Differential Diagnosis Algorithm
Infantile:
 • Benign Focal Epilepsy of Infancy
 • West
Causes of Pediatric ... Seizures - Differential ... Seizures #Epilepsy #Differential ... Diagnosis #Algorithm #Causes ... #Peds #Pediatrics
Gynecomastia - Differential Diagnosis Algorithm
No Testicular Mass on Ultrasound
 • Adrenal Neoplasm
 • Increased Extraglomerular Aromatase
Gynecomastia - Differential ... Tumor Normal T4 and ... Klinefelter's Syndrome ... Diagnosis #Algorithm #causes ... #endocrinology
Causes of Secondary Hypertension - Differential Diagnosis and Screening Testing
Common causes: 
 • Renal parenchymal disease
Hypertension - Differential ... disease - Renal ultrasound ... Duplex Doppler ultrasound ... • Cushing’s syndrome ... Screening #Workup #table
Schematic representation of the major sources of ammonia production and its excretory pathway (GI = gastrointestinal,
ammonia production and ... rare): - Reye syndrome ... (Peds) - Primary ... deficiency #Ammonia #Pathophysiology ... Hyperammonemia #Differential
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
: Pathogenesis and ... enzyme 21-OHase causes ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Causes of Secondary Hypertension - Workup and Differential Diagnosis
Approach (when evaluation should be done):
1. Severe or
Differential Diagnosis ... with previously stable ... Vasculitis • Endocrinologic ... White-coat syndrome ... #Differential #