7 results
diagnosis peds differential genetics causes iem inbornerrors metabolism neonatology nicu table 21hydroxylasedeficiency 21ohd adrenal cah comparison congenitaladrenalhyperplasia hypocalcemia interpretation laboratory
Lab patterns seen in Inborn Errors of Metabolism A table of lab values compiled from UpToDate and
Lab patterns seen ... values compiled ... from UpToDate and Pediatrics ... metabolicemergency-pathophysiology-differential-pediatrics-metabolism-algorithm-diagnosis ... Neonatology #Peds #Pediatrics
A schema of the pathophysiology of the inborn errors of metabolism, excluding complex storage diseases. Helps
See the lab values ... of information: Pediatrics ... , UpToDate #Pediatrics ... #Diagnosis #Algorithm ... Neonatology #Peds #Pediatrics
Approach to Thyroid Function Tests in the Evaluation of Hyperthyroidism • Low TSH, Low normal T4
• Low TSH, Low normal ... • Low TSH, normal ... Can repeat labs ... #algorithm #diagnosis ... #endocrinology
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
Short Stature - Differential Diagnosis Algorithm Normal Variant, Normal Puberty Onset (BA = CA) • Familial Short
Differential Diagnosis Algorithm ... Dwarfism) • Hypothyroidism ... Differential #Diagnosis #Algorithm ... #endocrinology ... #causes #pediatrics
Hypocalcemia - Differential Diagnosis Algorithm - Low and High PTH LOW PTH - Hypoparathyroid - Congenital (Pediatric)
Differential Diagnosis Algorithm ... - Congenital (Pediatric ... rhabdomyolysis, oral ... Differential #Diagnosis #Algorithm ... #PTH #endocrinology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
be labeled as males ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
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