9 results
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
congenital adrenal hyperplasia ... #CAH #algorithm ... #causes #pediatrics ... Endocrinology #Adrenal #pathophysiology
Bleeding and Bruising - Differential Diagnosis Algorithm
 • Vascular System Defect - Congenital vs Acquired
 •
Bleeding and Bruising ... - Differential ... Diagnosis Algorithm ... #Diagnosis #Algorithm ... #pathophysiology
Causes of Pediatric Wheezing - Differential Diagnosis Algorithm
CXR Abnormal:
 • Pulmonary Sequestration
 • Congenital Adenoid Cystic
Causes of Pediatric ... Wheezing - Differential ... Diagnosis Algorithm ... Fibrosis Wheeze With Feeding ... #Diagnosis #Algorithm
A schema of the pathophysiology of the inborn errors of metabolism, excluding complex storage diseases. Helps
schema of the pathophysiology ... of information: Pediatrics ... , UpToDate #Pediatrics ... #Diagnosis #Algorithm ... #Differential #
Causes of Abnormal Genital Bleeding - Differential Diagnosis Algorithm
Non-Gynecologic:
 • Medical (e.g. coagulopathy, liver disease, renal
Abnormal Genital Bleeding ... - Differential ... Diagnosis Algorithm ... • Endometrial Hyperplasia ... #Differential #
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
Causes of Sudden Unexpected Death in Infancy (SUDI) - Differential Diagnosis Algorithm
Congenital Anomaly / Disorder:
 •
Infancy (SUDI) - Differential ... Diagnosis Algorithm ... Infancy #Infant #Differential ... #Diagnosis #Algorithm ... #Causes #Peds #Pediatrics
Short Stature - Differential Diagnosis Algorithm
Normal Variant, Normal Puberty Onset (BA = CA)
 • Familial Short
Short Stature - Differential ... Diagnosis Algorithm ... Congenital Adrenal Hyperplasia ... #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
congenital adrenal hyperplasia ... • Early: decr feeding ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds #pediatrics