2 results
21hydroxylasedeficiency 21ohd diagnosis genetics neurology pediatrics physicalexam
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... Signs/Symptoms/Complications ... #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 ... safe to stop 2. ... Supraorbital pressure 2. ... • Examine for signs ... Casey Albin MD @
No results found for "2 classification pathophysiology causes signs peds endocrinology crisis fever comatose"
Try removing search terms or sorting by relevance
Or Upload an image for you and others searching for #2 #classification #pathophysiology #causes #signs #peds #endocrinology #crisis #fever #comatose