# Making the impossible possible: Baby KJ and the road map to personalized gene‐editing care

**Authors:** Vanessa Almendro, Sadik H. Kassim

PMC · DOI: 10.1002/ctm2.70515 · 2025-10-30

## Full-text entities

- **Genes:** CPS1 (carbamoyl-phosphate synthase 1) [NCBI Gene 1373] {aka CPS1D, CPSASE1, GATD6, PHN}
- **Diseases:** urea cycle disorders (MESH:D056806), hyperammonemia (MESH:D022124), monogenic diseases (MESH:D004194), neuromuscular disease (MESH:D009468), genetic disorders (MESH:D030342), monogenic disorders (MESH:D009358), neurotoxic (MESH:D020258), Batten disease (MESH:D009472), Carbamoyl phosphate synthetase 1 deficiency (MESH:D020165), neurological compromise (MESH:D009461), death (MESH:D003643)
- **Chemicals:** Lipid (MESH:D008055), oligonucleotides (MESH:D009841), nitrogen (MESH:D009584), ammonia (MESH:D000641), cGMP (MESH:D006152)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12572943/full.md

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Source: https://tomesphere.com/paper/PMC12572943