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21hydroxylasedeficiency endocrinology genetics peds physicalexam pisa pleurothotonus posture syndrome
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 ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology ... endocrinology #peds #pediatrics
Pisa Syndrome (pleurothotonus) on Physical Exam A tonic flexion of the trunk of the body to one
Pathophysiology: ... Treatment: anticholinergics ... #PhysicalExam #clinical ... #neurology #posture ... #video
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