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diagnosis peds 21hydroxylasedeficiency 21ohd algorithm cah comatose comparison congenitaladrenalhyperplasia evaluation examination genetics infant insufficiency laboratory neurology newborn testing treatment workup
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
of congenital adrenal ... CAH #algorithm #causes ... #pediatrics #CongenitalAdrenalHyperplasia ... treatment #Peds #Endocrinology ... #Adrenal #pathophysiology
Primary Adrenal Insufficiency: • ACTH stimulation test - Synthetic ACTH does not stimulate cortisol secretion because
ACTH stimulation test ... aldosterone - Low in cases ... in which injury ... autoantibody tests ... diagnosis #testing #endocrinology
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 ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
The Neurological Evaluation of a Comatose Patient Definition: • Coma: a state of unresponsiveness; the absence of
• Mutism Pathophysiology ... : • Severe injury ... Awareness • Injury ... Casey Albin MD @ ... caseyalbin #PhysicalExam
Newborn Infant - Routine Examination Birthweight, gestational age and birthweight percentile are noted. General observation Of the baby's
assessment, is best ... intra-abdominal masses ... which are usually renal ... Newborn #Infant #PhysicalExam ... Examination #Peds #Pediatrics
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