Argininemia

Argininemia
Other names: Arginase deficiency[1]
2D chemical structure of arginine
Arginine
SymptomsLethargy, Dehydration[2][3]
CausesMutations in the ARG1 gene[4][5]
Diagnostic methodUrinary orotic acid concentration[2]
TreatmentLimited protein intake, sodium benzoate[3]

Argininemia is an autosomal recessive urea cycle disorder where a deficiency of the enzyme arginase causes a buildup of arginine and ammonia in the blood. Ammonia, which is formed when proteins are broken down in the body, is toxic if levels become too high; the nervous system is especially sensitive to the effects of excess ammonia.[2][6]

Signs and symptoms

The presentation of argininemia, in those that are affected, is consistent with the following:[2][3]

Genetics

Argininemia has an autosomal recessive pattern of inheritance.

Mutations in the ARG1 gene cause argininemia, which belongs to a class of genetic diseases called urea cycle disorders.[4][5] The urea cycle is a sequence of reactions that occurs in liver cells (hepatocytes). This cycle processes excess nitrogen, generated when protein is used by the body, making urea that is excreted via the kidneys.[7]

The ARG1 gene provides instructions for making an enzyme called arginase, this enzyme controls the last steps of the urea cycle, which produces urea by extracting nitrogen from arginine.[4] In people with arginase deficiency, arginase is missing, and arginine is not broken down properly. consequently, urea cannot be produced and excess nitrogen accumulates in the blood in the form of ammonia. Ammonia and arginine are thought to cause neurological problems and other symptoms of arginase deficiency.[2]

This condition is an autosomal recessive disorder, which means the defective gene is located on an autosome,[6] and two copies of the defective gene are required to inherit the disorder.

Both parents of an individual with an autosomal recessive disorder are carriers of one copy of the gene, but usually do not have the disorder.

Diagnosis

MRI image showing hyperintense lesions in both frontal regions

The diagnosis for argininemia can usually be done using fetal blood sample.[8] One can look for the following indicators as to the presence of the condition:[2]

Treatment

Glycerol phenylbutyrate

The treatment for infants (individuals) with argininemia is the following, including medications:[3]

References

  1. ↑ Online Mendelian Inheritance in Man (OMIM): 207800
  2. 1 2 3 4 5 6 Wong, Derek; Cederbaum, Stephen; Crombez, Eric A. (1 January 1993). "Arginase Deficiency". GeneReviews. PMID 20301338. Archived from the original on 16 January 2021. Retrieved 20 November 2016.update 2014
  3. 1 2 3 4 "Arginase Deficiency: Background, Pathophysiology, Epidemiology". eMedicine. 15 April 2016. Archived from the original on 28 November 2016. Retrieved 28 November 2016.
  4. 1 2 3 Reference, Genetics Home. "ARG1 gene". Genetics Home Reference. Archived from the original on 28 November 2016. Retrieved 28 November 2016.
  5. 1 2 Ah Mew, Nicholas; Lanpher, Brendan C.; Gropman, Andrea; Chapman, Kimberly A.; Simpson, Kara L.; Summar, Marshall L. (1 January 1993). "Urea Cycle Disorders Overview". GeneReviews. PMID 20301396. Archived from the original on 3 February 2023. Retrieved 20 November 2016.update 2015
  6. 1 2 Reference, Genetics Home. "arginase deficiency". Genetics Home Reference. Archived from the original on 21 November 2016. Retrieved 20 November 2016.
  7. ↑ Hames, David; Hooper, Nigel (2005). Instant Notes in Biochemistry. Annales de Biologie Clinique. Vol. 58 (3rd ed.). Hoboken: Taylor & Francis Ltd. p. 408. ISBN 9780203967621. PMID 11098183. Retrieved 28 November 2016.
  8. ↑ Wyllie, Robert; Hyams, Jeffrey S.; Kay, Marsha (2015). Pediatric Gastrointestinal and Liver Disease. Elsevier Health Sciences. p. 886. ISBN 9780323370219. Archived from the original on 2023-07-12. Retrieved 2023-04-01.

Further reading

Classification
External resources
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