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diagnosis pediatrics infant pathophysiology treatment 21hydroxylasedeficiency 21ohd addiction adrenal buprenorphine comparison congenitaladrenalhyperplasia examination genetics initiation inpatient management newborn opiate physicalexam
Algorithm for the evaluation of the crying infant #Diagnosis #EM #Peds #Crying #Infant #Algorithm
Algorithm for the ... evaluation of the crying ... infant #Diagnosis #EM ... #Peds #Crying # ... Infant #Algorithm
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
#CAH #algorithm ... #causes #pediatrics ... comparison #treatment #Peds ... #Endocrinology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
mutation in CYP21A2 coding ... enzyme 21-OHase causes ... varying degrees ... pathophysiology #genetics #endocrinology ... #peds #pediatrics
Newborn Infant - Routine Examination Birthweight, gestational age and birthweight percentile are noted. General observation Of the baby's
the baby is not crying ... retinal vessels can ... intra-abdominal masses ... This can be confirmed ... #Examination #Peds
Quick Guide: Buprenorphine Initiation Algorithm Adjunctive meds: The following can be prescribed PRN for symptoms of withdrawal
Buprenorphine Initiation Algorithm ... Adjunctive meds ... The following can ... q 6 hours PRN nausea ... hold additional dosing
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