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21hydroxylasedeficiency diagnosis genetics neurology pediatrics peds physicalexam
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
: Pathogenesis and ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology ... #genetics #endocrinology
The Neurological Evaluation of a Comatose Patient Definition: • Coma: a state of unresponsiveness; the absence of
Evaluation of a Comatose ... • Mutism Pathophysiology ... • Vestibulo-ocular ... pontine lesion • Roving ... • Examine for signs
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