9 results
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
#CAH #algorithm ... #causes #pediatrics ... treatment #Peds #Endocrinology ... #Adrenal #pathophysiology
Lab patterns seen in Inborn Errors of Metabolism

A table of lab values compiled from UpToDate and
from UpToDate and Pediatrics ... See IEM schema for ... metabolicemergency-pathophysiology-differential-pediatrics-metabolism-algorithm-diagnosis ... Neonatology #Peds #Pediatrics ... NICU #Genetics #IEM
A schema of the pathophysiology of the inborn errors of metabolism, excluding complex storage diseases. Helps
of information: Pediatrics ... , UpToDate #Pediatrics ... #Diagnosis #Algorithm ... Neonatology #Peds #Pediatrics ... #Table #IEM #NICU
Causes of Pediatric Spells - Differential Diagnosis Algorithm
Neonates and Infant Spells:
 • Benign Sleep Myoclonus
 •
Causes of Pediatric ... Differential Diagnosis Algorithm ... Torticollis • Night Terrors ... #Causes #Peds # ... Pediatrics
Causes of Chronic Pediatric Cough - Differential Diagnosis Algorithm
Poor Growth
 - Non-Specific CXR
Causes of Chronic ... Pediatric Cough ... Scan: • Tumors ... #Causes #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 ... #Neonatology #IDM ... OBGYN #Diagnosis #Pathophysiology
Short Stature - Differential Diagnosis Algorithm
Normal Variant, Normal Puberty Onset (BA = CA)
 • Familial Short
Differential Diagnosis Algorithm ... Nervosa • CNS Tumors ... Differential #Diagnosis #Algorithm ... #endocrinology ... #causes #pediatrics
Causes of Pediatric Seizures - Differential Diagnosis Algorithm
Infantile:
 • Benign Focal Epilepsy of Infancy
 • West
Causes of Pediatric ... Differential Diagnosis Algorithm ... Torticollis • Night Terrors ... #Causes #Peds # ... Pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics