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diagnosis algorithm pathophysiology 21hydroxylasedeficiency 21ohd cah comparison congenitaladrenalhyperplasia differential examination genetics newborn 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 #CongenitalAdrenalHyperplasia ... diagnosis #comparison #treatment ... #Peds #Endocrinology
Short Stature - Differential Diagnosis Algorithm Normal Variant, Normal Puberty Onset (BA = CA) • Familial Short
• Congenital Adrenal ... Panhypopituitarism Treatment ... Chronic UTI) • ... 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
enzyme 21-OHase causes ... 21-OHD in the adrenal ... deficiencies present in infants ... pathophysiology #genetics #endocrinology ... #peds #pediatrics
Newborn Infant - Routine Examination Birthweight, gestational age and birthweight percentile are noted. General observation Of the baby's
Newborn Infant - ... always needs urgent assessment ... intra-abdominal masses ... #Examination #Peds ... #Pediatrics #Diagnosis
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