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Yang, C. Arginase Deficiency. Encyclopedia. Available online: https://encyclopedia.pub/entry/4761 (accessed on 26 April 2024).
Yang C. Arginase Deficiency. Encyclopedia. Available at: https://encyclopedia.pub/entry/4761. Accessed April 26, 2024.
Yang, Catherine. "Arginase Deficiency" Encyclopedia, https://encyclopedia.pub/entry/4761 (accessed April 26, 2024).
Yang, C. (2020, December 24). Arginase Deficiency. In Encyclopedia. https://encyclopedia.pub/entry/4761
Yang, Catherine. "Arginase Deficiency." Encyclopedia. Web. 24 December, 2020.
Arginase Deficiency
Edit
This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/condition/arginase-deficiency

Arginase deficiency is an inherited disorder that causes the amino acid arginine (a building block of proteins) and ammonia to accumulate gradually 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.

genetic conditions

1. Introduction

Arginase deficiency usually becomes evident by about the age of 3. It most often appears as stiffness, especially in the legs, caused by abnormal tensing of the muscles (spasticity). Other symptoms may include slower than normal growth, developmental delay and eventual loss of developmental milestones, intellectual disability, seizures, tremor, and difficulty with balance and coordination (ataxia). Occasionally, high protein meals or stress caused by illness or periods without food (fasting) may cause ammonia to accumulate more quickly in the blood. This rapid increase in ammonia may lead to episodes of irritability, refusal to eat, and vomiting.

In some affected individuals, signs and symptoms of arginase deficiency may be less severe, and may not appear until later in life.

2. Frequency

Arginase deficiency is a very rare disorder; it has been estimated to occur once in every 300,000 to 1,000,000 individuals.

3. Causes

Mutations in the ARG1 gene cause arginase deficiency.

Arginase deficiency belongs to a class of genetic diseases called urea cycle disorders. The urea cycle is a sequence of reactions that occurs in liver cells. This cycle processes excess nitrogen, generated when protein is used by the body, to make a compound called urea that is excreted by the kidneys.

The ARG1 gene provides instructions for making an enzyme called arginase. This enzyme controls the final step of the urea cycle, which produces urea by removing nitrogen from arginine. In people with arginase deficiency, arginase is damaged or missing, and arginine is not broken down properly. As a result, urea cannot be produced normally, and excess nitrogen accumulates in the blood in the form of ammonia. The accumulation of ammonia and arginine are believed to cause the neurological problems and other signs and symptoms of arginase deficiency.

3.1. The gene associated with Arginase deficiency

  • ARG1

4. Inheritance

This condition is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically do not show signs and symptoms of the condition.

5. Other Names for This Condition

  • ARG1 deficiency

  • Arginase Deficiency Disease

  • Argininemia

  • Hyperargininemia

References

  1. Ah Mew N, Simpson KL, Gropman AL, Lanpher BC, Chapman KA, Summar ML. UreaCycle Disorders Overview. 2003 Apr 29 [updated 2017 Jun 22]. In: Adam MP,Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors.GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle;1993-2020. Available from http://www.ncbi.nlm.nih.gov/books/NBK1217/
  2. Crombez EA, Cederbaum SD. Hyperargininemia due to liver arginase deficiency.Mol Genet Metab. 2005 Mar;84(3):243-51.
  3. Endo F, Matsuura T, Yanagita K, Matsuda I. Clinical manifestations of inbornerrors of the urea cycle and related metabolic disorders during childhood. JNutr. 2004 Jun;134(6 Suppl):1605S-1609S; discussion 1630S-1632S, 1667S-1672S.doi: 10.1093/jn/134.6.1605S. Review.
  4. Scaglia F, Brunetti-Pierri N, Kleppe S, Marini J, Carter S, Garlick P, Jahoor F, O'Brien W, Lee B. Clinical consequences of urea cycle enzyme deficiencies and potential links to arginine and nitric oxide metabolism. J Nutr. 2004 Oct;134(10 Suppl):2775S-2782S; discussion 2796S-2797S. doi: 10.1093/jn/134.10.2775S. Review.
  5. Sun A, Crombez EA, Wong D. Arginase Deficiency. 2004 Oct 21 [updated 2020 May 28]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K,Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University ofWashington, Seattle; 1993-2020. Available fromhttp://www.ncbi.nlm.nih.gov/books/NBK1159/
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Subjects: Genetics & Heredity
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Catherine Yang
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Entry Collection: MedlinePlus
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Update Date: 24 Dec 2020
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