| 11. | Mutations in " MUT " gene may lead to various types of methylmalonic aciduria.
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| 12. | In peroxisomes, the accumulation of this substance causes malonic aciduria, a highly pathogenic disease.
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| 13. | Urocanic aciduria is thought to be relatively benign . no definitive neurometabolic connection has yet been established.
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| 14. | The metabolic disease was found to be on a unsaturated dicarboxylic acids, a condition called dicarboxylic aciduria.
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| 15. | The incidence of 3-methylglutaconic aciduria type II is approximately 1 in 200, 000 male infants.
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| 16. | Uridine triacetate is a drug approved by FDA to be used in the treatment of hereditary orotic aciduria.
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| 17. | Glutaric aciduria type 1, in many cases, can be defined as a cerebral palsy of genetic origins.
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| 18. | Mutations in the L2HGDH gene cause L-2-hydroxyglutaric aciduria, a rare autosomal recessive neurometabolic disorder.
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| 19. | Mutations in IDH2 are associated with 2-hydroxyglutaric aciduria, a condition that causes progressive damage to the brain.
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| 20. | Mutations in the gene are the cause of vitamin B 12-dependent methylmalonic aciduria linked to the cblB complementation group.
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