Propionic acidemia definition

Propionic acidemia means a congenital disorder characterized by an accumulation of glycine and 3-hydroxypropionic acid due to defective propionyl-CoA carboxylase activity.
Propionic acidemia means a congenital disorder char- acterized by an accumulation of glycine and 3-hydroxy- propionic acid due to defective propionyl-CoA carboxylase activity.
Propionic acidemia means a congenital disorder characterized by an accumulation of glycine and 3-hydroxy- propionic acid due to defective propionyl-CoA carboxylase activity.

Examples of Propionic acidemia in a sentence

  • A fee of nine cents ($.09) per deduction shall be assessed by the Controller for the processing of each PAC deduction taken.

  • Formulas for the treatment of inborn diseases of metabolism of amino acids and organic acids such as:• Phenylketonuria (PKU);• Tyrosinemia;• Homocystinuria;• Maple syrup urine disease;• Propionic acidemia or methylmalonic acidemia; or• Methylmalonic acidemia.

  • Medical foods for the treatment of inherited enzymatic disorders caused by single gene defects, including but not limited to: Phenylketonuria. Maternal phenylketonuria Maple syrup urine disease. Hyperlysinemia. Glutaric acidemia. Methylmalonic acidemia. Propionic acidemia.

  • Propionic acidemia, a genetical inherent disorder may lead to severe health implications and is correlated with mental retardation, mitochondrial dysfunction and other health problems (Khalesi and Garshasbi, 2017, MacFabe, 2012).

  • Propionic acidemia: neonatal versus selective metabolic screening.

  • Propionic acidemia (PA) (mRNA-3927): Study start-up activities for the Phase 1/2 study of PA candidate (mRNA-3927) have resumed following COVID-19 related pause and protocol amendment.

  • Medical consultant phones practitioner with follow-up recommendations.C3 (Propionyl) >7.50 µM/L C3/C2 >0.30 µM/L* Methylmalonic acidemias possible* Multiple carboxylase deficiency possible* Propionic acidemia possible* False positiveNBS nurse faxes results.

  • Specific treatment include cofactor biotin and Propimex-1 formula for Propionic acidemia, Thiamine and Ketonex-1 formula for Maple syrup urine disease, High carbohydrate diet and biotin for Pyruvate carboxylase deficiency etc.

  • Systemic Intracellular Therapeutics: These programs aim to deliver mRNA into cells within target organs as a therapeutic approach for diseases caused by a missing or defective protein.• Propionic acidemia (PA) (mRNA-3927): The Phase 1/2 Paramount study of mRNA-3927 is ongoing and the first cohort is fully enrolled.

  • One of the most critical areas that require improvement is the M&E system.


More Definitions of Propionic acidemia

Propionic acidemia means a congenital disorder characterized by an accumulation of glycine and 3-hydroxypropi-
Propionic acidemia means a congenital disorder characterized by an accumulation of glycine and 3-hydroxypropi- onic acid due to defective propionyl-CoA carboxylase activity.

Related to Propionic acidemia

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