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21hydroxylasedeficiency 21ohd cord diagnosis differential disorders genetics pathophysiology peds spinal spinalcord
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 ... pathophysiology #genetics #endocrinology ... #peds #pediatrics
Spinal Cord Disorders - Differential Diagnosis Framework Spinal cord neurological lesion: Clinical findings: • Symptoms and signs below
neurological lesion: Clinical ... and signs below ... MCTD, Sjogren syndrome ... disorders #diagnosis #neurology ... differential #algorithm
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