Indeed, there are case reports of monozygotic twins harboring the exact same mutation, both with elevated serum very long chain fatty acids (indicating a similar metabolic defect of peroxisomal lipid processing), where one boy is affected clinically and radiologically, while his twin brother is completely normal (Korenke et al., 1996)
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7.1 Advancing detection and risk assessment technologies Emerging analytical technologies offer unprecedented opportunities to improve EED detection sensitivity, exposure assessment accuracy, and biomonitoring precision across diverse populations and exposure scenarios
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