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differential causes genetics 21hydroxylasedeficiency 21ohd cah comparison congenitaladrenalhyperplasia failuretothrive ftt hypocalcemia iem inbornerrors incomplete kawasaki lowcalcium metabolicemergency metabolism neonatology nicu
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
#CAH #algorithm ... #causes #pediatrics ... comparison #treatment #Peds ... #Endocrinology ... #Adrenal #pathophysiology
A schema of the pathophysiology of the inborn errors of metabolism, excluding complex storage diseases. Helps
schema of the pathophysiology ... complex storage diseases ... #Diagnosis #Algorithm ... #Neonatology #Peds ... #Pediatrics #Table
Short Stature - Differential Diagnosis Algorithm Normal Variant, Normal Puberty Onset (BA = CA) • Familial Short
- Differential Diagnosis ... Algorithm Normal ... • Cushing's Disease ... #Algorithm #endocrinology ... #causes #pediatrics
Hypocalcemia - Differential Diagnosis Algorithm - Low and High PTH LOW PTH - Hypoparathyroid - Congenital (Pediatric)
- Differential Diagnosis ... Algorithm - Low ... - Congenital (Pediatric ... • Chronic Renal ... #endocrinology
Causes of Failure to Thrive - Differential Diagnosis Algorithm Adequate Calorie Consumption - Increased Losses:
- Differential Diagnosis ... Algorithm Adequate ... • Celiac Disease ... • Liver Disease ... #Peds #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 ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Evaluation of suspected incomplete Kawasaki Disease 1. AHA consensus recommendations 2. Infants ≤6 months old on day ≥7
incomplete Kawasaki Disease ... clinical and lab signs ... #Diagnosis #Peds ... #Pediatrics #Kawasaki ... #Algorithm
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