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diagnosis genetics management 21hydroxylasedeficiency amyotrophic differential endocrinology kernigs meningitis myelitis physicalexam praderwilli sclerosis syndrome transverse
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
clinical findings ... Prader-Willi Syndrome Signs ... /Symptoms/Complications ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
Kernig's Sign in Meningitis Kernig's sign is present if the patient, in the supine position with the
Kernig's Sign in ... Meningitis Kernig's sign ... Prakash #Kernigs #Sign ... #Pediatrics #Peds ... #neurology
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 21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Clinical Findings ... • This is also ... Signs/Symptoms/Complications ... #pathophysiology ... #pediatrics
Amyotrophic Lateral Sclerosis (ALS) Summary ALS: combination of the clinical examination finding of amyotrophy with the pathologic
LMN signs in the ... LMN signs to determine ... LMN signs on examination ... EMG: LMN Signs in ... #Sclerosis #neurology
Transverse Myelitis Overview Focal inflammatory disorder of the spinal cord resulting in rapid onset of weakness, sensory
monophasic Pathophysiology ... Transverse Myelitis - Clinical ... Hyperreflexia develops later ... signs and/or symptoms ... diagnosis #management #neurology
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