# Treatment and Improved Outcomes of Three Adult Patients With Guanidinoacetate Methyltransferase (GAMT) Deficiency

**Authors:** Angela Lee, Judith Weisenberg, Elizabeth Toolan, Marwan Shinawi

PMC · DOI: 10.1002/jmd2.70019 · 2025-05-05

## TL;DR

Three adults with GAMT deficiency showed improved outcomes with treatment, stressing the importance of early and continued care.

## Contribution

The study highlights the long-term benefits of treatment initiation in early childhood and the need for ongoing management in adulthood.

## Key findings

- Early treatment at 14 months led to near-normal neurocognitive outcomes.
- Continued treatment is necessary for managing GAMT deficiency into adulthood.
- More research is needed to determine optimal treatment strategies for adults.

## Abstract

Guanidinoacetate methyltransferase (GAMT) deficiency is a creatine synthesis disorder caused by biallelic pathogenic variants in GAMT. Early diagnosis and treatment can lead to normal neurocognitive outcomes, which has prompted its recent addition to the Recommended Uniform Screening Panel. Treatment typically includes creatine and ornithine supplementation, with or without arginine restriction or sodium benzoate. Here, we present the clinical outcomes of 3 adult patients with GAMT deficiency who began creatine and ornithine supplementation at varying ages. One patient started on treatment at 14 months of age and has had near‐normal neurocognitive outcomes, highlighting the positive clinical impact of early treatment. Our findings also emphasize the need to continue treatment throughout adulthood, but further research is required to understand the natural history and determine the optimal treatment of GAMT deficiency in adults.

## Linked entities

- **Genes:** GAMT (guanidinoacetate N-methyltransferase) [NCBI Gene 2593]
- **Chemicals:** creatinine (PubChem CID 588), ornithine (PubChem CID 389), arginine (PubChem CID 232), sodium benzoate (PubChem CID 517055)
- **Diseases:** GAMT deficiency (MONDO:0012999)

## Full-text entities

- **Diseases:** GAMT deficiency (MESH:C537622), creatine synthesis disorder (MESH:C535598)
- **Chemicals:** creatine (MESH:D003401), arginine (MESH:D001120), ornithine (MESH:D009952), sodium benzoate (MESH:D020160)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12053078/full.md

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Source: https://tomesphere.com/paper/PMC12053078