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diagnosis pathophysiology 21hydroxylasedeficiency 21ohd bruising cah comparison congenitaladrenalhyperplasia differential disease examination facial genetics incomplete infant kawasaki physicalexam shortstature
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
of congenital adrenal ... #CAH #algorithm ... #causes #pediatrics ... diagnosis #comparison #treatment ... #Peds #Endocrinology
This is another example of facial bruising. Here again the face appears to be cyanotic (including
bruising in a newborn ... ; no further evaluation ... facial #bruising #newborn ... #peds #pediatrics ... #clinical #photo
Short Stature - Differential Diagnosis Algorithm Normal Variant, Normal Puberty Onset (BA = CA) • Familial Short
Differential Diagnosis Algorithm ... • Congenital Adrenal ... Panhypopituitarism Treatment ... #endocrinology ... #causes #pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... enzyme 21-OHase causes ... 21-OHD in the adrenal ... pathophysiology #genetics #endocrinology ... #peds #pediatrics
Evaluation of suspected incomplete Kawasaki Disease 1. AHA consensus recommendations 2. Infants ≤6 months old on day ≥7
Evaluation of suspected ... if they have no clinical ... echo is positive, treatment ... #Diagnosis #Peds ... #Pediatrics #Kawasaki
Newborn Infant - Routine Examination Birthweight, gestational age and birthweight percentile are noted. General observation Of the baby's
Newborn Infant - ... requires further evaluation ... #Newborn #Infant ... #Examination #Peds ... #Pediatrics #Diagnosis
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