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diagnosis differential pathophysiology pediatrics 21hydroxylasedeficiency 21ohd disorders endocrinology management myelitis physicalexam praderwilli reflex spinal spinalcord syndrome transverse tromners video
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
clinical findings ... Prader-Willi Syndrome Signs ... , sleep apnea, cor ... PraderWilli #Syndrome #genetics ... pathophysiology #peds
Tromner Sign on Physical Exam The Trömner sign is commonly used as a clinical neurological examination for
Tromner Sign on ... The Trömner sign ... of the spinal cord ... #Tromners #Sign ... #Video #Neurology
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 Spinal Cord Disorders - Differential Diagnosis Framework Spinal cord neurological lesion: Clinical findings: • Symptoms and signs below
Spinal Cord Disorders ... neurological lesion: Clinical ... signs below the ... disorders #diagnosis #neurology ... differential #algorithm
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
: Pathogenesis and ... Clinical Findings ... Signs/Symptoms/Complications ... pathophysiology #genetics ... endocrinology #peds
Transverse Myelitis Overview Focal inflammatory disorder of the spinal cord resulting in rapid onset of weakness, sensory
of the spinal cord ... Transverse Myelitis - Clinical ... extensors of the arms (pyramidal ... • Bilateral signs ... diagnosis #management #neurology
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