Treating hyperammonemia due to NAGS deficiency

Be prepared to act quickly to diagnose this serious, rare genetic disorder that can present suddenly in neonates and suddenly or chronically in individuals with late-onset NAGS deficiency (NAGSD). Rapid progression to a hyperammonemic crisis can occur in anyone with the disorder. Prescribe your patients an FDA-approved proven treatment that can be the key to normalizing high blood ammonia levels.

Review CARBAGLU® (carglumic acid) clinical data

You and your patients can learn more about the urea cycle, NAGS deficiency, and the importance of normalizing high blood ammonia levels.

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Diagnosing hyperammonemia due to NAGSD

Hyperammonemic crises can result in serious neurological complications and death. Clinicians must act quickly to diagnose and treat.1

Identify symptoms and review diagnostic tests

CARBAGLU clinical results

CARBAGLU has been shown to normalize high blood ammonia levels.

Review clinical data

References

  1. Cartagena A, Prasad AN, Rupar CA, Strong M, Tuchman M, Ah Mew N, Prasad C. Recurrent encephalopathy: NAGS (N-acetylglutamate synthase) deficiency in adults. Can J Neurol Sci. 2013;40:3-9.
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