key clinical sign management pivot symptoms differential deficiency endocrinology signs 21hydroxylasedeficiency genetics

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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 ... a scrotum #21HydroxylaseDeficiency ... pathophysiology #genetics ... #endocrinology

Transverse Myelitis Overview

Focal inflammatory disorder of the spinal cord resulting in rapid onset of weakness, sensory

Transverse Myelitis - Clinical ... • Bilateral signs ... and/or symptoms ... • Nutritional Deficiency ... #neurology #differential

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