AUTHOR AND EDITOR INFORMATION

Section 1 of 11  

• Authors and Editors
• Introduction
• Clinical
• Differentials
• Workup
• Treatment
• Medication
• Follow-up
• Miscellaneous
• Multimedia
• References

INTRODUCTION

Section 2 of 11  

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• Introduction
• Clinical
• Differentials
• Workup
• Treatment
• Medication
• Follow-up
• Miscellaneous
• Multimedia
• References

Background

Normal enzyme function of N-acetylglutamate synthetase (NAGS) deficiency is confined to the hepatic mitochondria and mediates the reaction acetyl-coenzyme A (CoA) + glutamate ® N-acetylglutamate + CoA. As a mitochondrial reaction, each of the substrates normally is omnipresent. Acetyl-CoA is a cofactor in many mitochondrial reactions, and glutamate is the transamination product of a-ketoglutarate and alanine; a-ketoglutarate is produced by the Krebs cycle.

The normal function of N-acetylglutamate (NAG), the reaction product, is to act as an activator of carbamyl phosphate synthetase (CPS) (see Media file 1), which is also a mitochondrial enzyme. The activation process requires physical binding of NAG to the CPS enzyme, in turn, causing the inactive form of CPS to convert to an active state. Thus, CPS activity is regulated by the relationship of available NAG to inactive CPS enzyme protein.

The biochemical effect of NAGS deficiency is an inability to form adequate NAG; this results in failure to activate the enzyme responsible for the reaction NH₄⁺ + CO₂ + ATP ® H₂N-CO-PO₃^2- + ADP, which is the entry step into the urea cycle (see Carbamyl Phosphate Synthetase Deficiency).

Clinical signs and symptoms of NAGS deficiency occur when ammonia fails to fix into carbamoyl phosphate (CP) effectively, thus disabling the urea cycle. This leads to accumulation of alanine and glutamine (transamination products of pyruvate and glutamate, respectively) and, finally, of ammonia. The condition is progressive without intervention.

Pathophysiology

Overall, the hepatic urea cycle is the major route for waste nitrogen disposal, generation of which is chiefly from protein and amino acid metabolism. Low-level synthesis of certain cycle intermediates in extrahepatic tissues makes a small contribution to waste nitrogen disposal as well. A portion of the cycle is mitochondrial in nature; mitochondrial dysfunction may impair urea production and result in Hyperammonemia. Overall, activity of the cycle is regulated by the rate of synthesis of NAG, the enzyme activator that initiates incorporation of ammonia into the cycle.

Frequency

United States

Too few cases have been reported to cite any incidence figures. However, there has been an increasing recognition of affected patients.

International

Only a handful of cases have been reported worldwide.

Mortality/Morbidity

NAGS deficiency is associated with significant morbidity and mortality. Patients who present with hyperammonemia are at risk for cerebral edema and death if treatment is not begun immediately. Survivors of hyperammonemic coma will likely suffer brain damage and resulting developmental delays, learning disabilities, and/or mental retardation.

Sex

Case reports of NAGS deficiency have shown the condition to occur in both sexes.

Age

NAGS deficiency can present at any age. As with many inherited metabolic diseases, the most likely time of presentation is in the newborn period.

CLINICAL

Section 3 of 11  

• Authors and Editors
• Introduction
• Clinical
• Differentials
• Workup
• Treatment
• Medication
• Follow-up
• Miscellaneous
• Multimedia
• References

History

• The multiple primary causes of hyperammonemia, specifically those due to urea cycle enzyme deficiencies, are somewhat variable in presentation, diagnostic features, and treatment. For these reasons, the family of urea cycle defects is considered individually in this article; however, the common denominator, hyperammonemia, can be manifested clinically by some or all of the following:
• • Anorexia
  • Irritability
  • Heavy or rapid breathing
  • Lethargy
  • Vomiting
  • Disorientation
  • Somnolence
  • Asterixis (rare)
  • Combativeness
  • Obtundation
  • Coma
  • Cerebral edema
  • Death if treatment is not forthcoming or effective
• As a consequence, the most striking clinical findings of each urea cycle disorder relate to this constellation of symptoms and rough temporal sequence of events.

Physical

• General
• • Signs of severe hyperammonemia may be present.
  • Poor growth may be evident.
• Head, ears, eyes, nose, and throat (HEENT): Papilledema may be present if cerebral edema and increased intracranial pressure have ensued.
• Pulmonary
• • Tachypnea or hyperpnea may be present.
  • Apnea and respiratory failure may occur in later stages.
• Abdominal: Hepatomegaly may be present and is usually mild.
• Neurologic
• • Poor coordination
  • Dysdiadochokinesia
  • Hypotonia or hypertonia
  • Ataxia
  • Tremor
  • Seizures and hypothermia
  • Lethargy progressing to combativeness to obtundation to coma
  • Decorticate or decerebrate posturing

Causes

• The pedigree distribution of reported cases supports an autosomal recessive inheritance pattern, and the growing numbers of reported cases confirm that this is the case.
• Nothing is known of the genetic basis of this condition.
• Urea cycle defects with resulting hyperammonemia are due to deficiencies of the enzymes involved in the metabolism of waste nitrogen. The enzyme deficiencies lead to disorders with nearly identical clinical presentations. The exception is arginase, the last enzyme of the cycle; arginase deficiency causes a somewhat different set of signs and symptoms.

DIFFERENTIALS

Section 4 of 11  

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Other Problems to be Considered

Lysinuric protein intolerance
Reye syndrome

WORKUP

Section 5 of 11  

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• Introduction
• Clinical
• Differentials
• Workup
• Treatment
• Medication
• Follow-up
• Miscellaneous
• Multimedia
• References

Lab Studies

• Ammonia level: Affected newborns may experience fulminant hyperammonemia, which will go undetected unless index of suspicion is high.
• No routine laboratory tests provide definitive clues.
• • The BUN level may be low, but this is an unreliable index of high blood ammonia.
  • A respiratory alkalosis may be present.
  • Urine orotic acid levels are within reference ranges.
• Blood amino acids: Plasma alanine and glutamine levels are elevated.
• Urine amino acids are nondiagnostic in NAGS but are important in order to help rule out hyperammonemia-hyperornithinemia-homocitrullinemia (HHH) or lysinuric protein intolerance (LPI) (see Differentials).
• Urine organic acids are within reference ranges in NAGS deficiency. Ruling out organic acid disorders, which can present with similar signs and symptoms and hyperammonemia, is important.

Imaging Studies

• Imaging studies generally are not helpful, with the exception of brain imaging when cerebral edema is suspected. Documenting a finding of cerebral edema is important.

Procedures

• Liver biopsy
• • A liver biopsy, best performed when the patient is stable, is essential for definitive diagnosis.
  • As a mitochondrial enzyme, it is quite labile; therefore, handle the specimen with scrupulous care and identify a laboratory prior to scheduling the biopsy that is capable of performing the enzymatic testing.

TREATMENT

Section 6 of 11  

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• Medication
• Follow-up
• Miscellaneous
• Multimedia
• References

Medical Care

• Immediate cessation of protein intake is mandatory in the face of high blood ammonia levels with provision of supplementary nonprotein energy to close the caloric gap. In most cases of severe hyperammonemia, the patient is given nothing enterally until the hyperammonemia is well controlled.
• Treatment of severe hyperammonemia is a true emergency.
• • Reduction of blood ammonia can usually be achieved with intravenous sodium benzoate and phenylacetate. Intravenous sodium benzoate and phenylacetate (Ammonul) was approved in the United States in February, 2005.
  • Alternatively, hemodialysis is usually effective in bringing down the ammonia level, especially with the initial presentation.
  • Exchange transfusion is ineffective and not generally recommended.
  • Intravenous fluids with glucose and sometimes arginine hydrochloride (HCl) added may be indicated.
  • Maintaining as high of an energy intake as possible is important.
• Specific therapy of NAGS following diagnosis rests upon dietary protein restriction and provision of arginine to enhance availability of ornithine and administration of carbamylglutamate (which is not widely available), a functional analogue of NAG. Some patients have done well using this regimen. Whether or not PO sodium phenylbutyrate is helpful in this condition is unclear.

Consultations

NAGS deficiency is an extremely rare disorder with complex treatment. Consultation with a metabolic disease/medical genetic specialist is usually necessary for assistance with laboratory diagnosis and clinical care. Contact these consultants by telephone if they are not available locally.

Diet

A low-protein diet is generally recommended with dietary supervision under the direction of a dietitian experienced in the care of patients with metabolic disease.

MEDICATION

Section 7 of 11  

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Drug Category: Metabolic analogue

In the absence of any ability to fix nitrogen generated from endogenous catabolism of protein, the urea cycle is of no use whatsoever to the homeostasis of nitrogen metabolism. In order to stimulate urea cycle action, investigators have used N-carbamoyl-L-glutamate as an analogue of N-acetyl-L-glutamate to activate CPS.

Drug Category: Metabolic agents

These agents assist in the excretion of nitrogen and serve as an alternative to urea to reduce waste nitrogen levels. Administer only in a large medical facility with close laboratory monitoring available.

FOLLOW-UP

Section 8 of 11  

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• Introduction
• Clinical
• Differentials
• Workup
• Treatment
• Medication
• Follow-up
• Miscellaneous
• Multimedia
• References

Further Outpatient Care

• The patient should be under the care of a biochemical geneticist (metabolic disease specialist) who is an expert in the care of patients with urea cycle defects.
• Make medication adjustments on the basis of continued growth and frequently measured plasma amino acids; include the input of a highly trained nutritionist.

Transfer

• Consider transferring the patient to a facility equipped for emergent hemodialysis (if the patient is a neonate) and where the appropriate consultants (see Consultations) are immediately available.

Complications

• Possible complications include cerebral edema with resulting brain damage or death.

Prognosis

• Long-term prognosis is unclear; most likely, the future IQ depends upon the severity of the initial presentation and the subsequent hyperammonemic episodes suffered.

Patient Education

• Family counseling
• • Inform parents of their obligate heterozygote status given the likelihood that this is an autosomal recessive trait.
  • Parents must understand that the chance of recurrence is 1:4 (25%) with each subsequent pregnancy.
  • Advise parents to seek early medical attention for the patient in the event of intercurrent illness.

MISCELLANEOUS

Section 9 of 11  

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• Clinical
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• Workup
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• Follow-up
• Miscellaneous
• Multimedia
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Medical/Legal Pitfalls

• Always measure an ammonia level immediately in a patient of any age with unexplained lethargy or coma.
• Treat new onset hyperammonemia aggressively and immediately with advice from experts.
• Usual treatments for hyperammonemia, such as lactulose, are totally ineffective in patients with urea cycle disorders.

MULTIMEDIA

Section 10 of 11  

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• Introduction
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• Differentials
• Workup
• Treatment
• Medication
• Follow-up
• Miscellaneous
• Multimedia
• References

Media file 1:  Compounds comprising the urea cycle are numbered sequentially, beginning with carbamyl phosphate (1). At this step, the first waste nitrogen is incorporated into the cycle; it is also at this step that N-acetylglutamate exerts its regulatory control on the mediating enzyme, carbamyl phosphate synthetase (CPS). Compound 2 is citrulline, the product of condensation between carbamyl phosphate (1) and ornithine (8); the mediating enzyme is ornithine transcarbamylase. Compound 3 is aspartic acid, which is combined with citrulline to form argininosuccinic acid (ASA) (4); the reaction is mediated by ASA synthetase. Compound 5 is fumaric acid generated in the reaction that converts ASA to arginine (6), which is mediated by ASA lyase.
	View Full Size Image
Media type:  Graph

REFERENCES

Section 11 of 11

• Authors and Editors
• Introduction
• Clinical
• Differentials
• Workup
• Treatment
• Medication
• Follow-up
• Miscellaneous
• Multimedia
• References

• Bachmann C. N-acetylglutamate synthetase deficiency: diagnosis, clinical observations and treatment. Adv Exp Med Biol. 1981;153:39-46.
• Caldovic L, Morizono H, Panglao MG, et al. Null mutations in the N-acetylglutamate synthase gene associated with acute neonatal disease and hyperammonemia. Hum Genet. Apr 2003;112(4):364-8. [Medline].
• Elpeleg O, Shaag A, Ben-Shalom E. N-acetylglutamate synthase deficiency and the treatment of hyperammonemic encephalopathy. Ann Neurol. 2002;52:845-849.
• Elpeleg ON, Colombo JP, Amir N, et al. Late-onset form of partial N-acetylglutamate synthetase deficiency. Eur J Pediatr. Jun 1990;149(9):634-6. [Medline].
• Guffon N, Vianey-Saban C, Bourgeois J, et al. A new neonatal case of N-acetylglutamate synthase deficiency treated by carbamylglutamate. J Inherit Metab Dis. 1995;18(1):61-5. [Medline].
• Guffon N, Schiff M, Cheillan D. Neonatal hyperammonemia: the N-carbamoyl-L-glutamic acid test. J Pediatr. 2005;147:260-262.
• Haberle J, Koch HG. Genetic approach to prenatal diagnosis in urea cycle defects. Prenat Diagn. 2004;24:378-383.
• Plecko B, Erwa W, Wermuth B. Partial N-acetylglutamate synthetase deficiency in a 13-year-old girl: diagnosis and response to treatment with N-carbamylglutamate. Eur J Pediatr. Dec 1998;157(12):996-8. [Medline].

Article Last Updated: Mar 16, 2006