4 results
diagnosis neurology spinalcord 21hydroxylasedeficiency 21ohd acute als amyotrophic cord differential disorders endocrinology genetics injury lateral management msk orthopedics peds sclerosis
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 ... non-arousable, decr urine ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds #pediatrics
Acute Spinal Cord Injuries: Pathogenesis and clinical findings • Anterior Cord Syndrome -> Anterior spinal artery
Pathogenesis and clinical ... injury, often from vascular ... Syndromes #diagnosis #pathophysiology ... #signs #symptoms ... #orthopedics #neurology
Spinal Cord Disorders - Differential Diagnosis Framework Spinal cord neurological lesion: Clinical findings: • Symptoms and signs below
neurological lesion: Clinical ... and signs below ... Vascular/Blockage ... disorders #diagnosis #neurology ... differential #algorithm
Amyotrophic Lateral Sclerosis (ALS) Summary ALS: combination of the clinical examination finding of amyotrophy with the pathologic
combination of the clinical ... lateral sclerosis Pathophysiology ... 4) progressive muscular ... fasciculations Common Symptoms ... Lateral #Sclerosis #neurology
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