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21hydroxylasedeficiency algorithm endocrinology genetics head injury pathophysiology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... Signs/Symptoms/Complications ... vomiting • Late (shock ... endocrinology #peds ... #pediatrics
Algorithm for Management of Head Injuries in Children Primary survey: • Airway and cervical spine • Breathing
Algorithm for Management ... of vomiting • Clinical ... fontanelle • Sign ... trama #pediatrics ... #peds
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