A study of Iraqi patients with homocysteine remethylation disorders in a tertiary pediatric centre
According to this study, individuals with homocysteine re-methylation disorders can manifest symptomatology such as neuroregression, psychomotor delay, and whiter matter changes earlier than anticipated. And these disorders are amenable to treatment. Genetic testing is crucial in identifying the specific mutation type and guiding definitive treatment.
Authors
- Adel A. Kareem
- Mohamed Altai (ORCID: https://orcid.org/0000-0002-7624-0313)
- Tawfeg Ben Omran
- Nebal Waill Saadi
- Ibrahim F. Ibrahim
- Lamia A. Alattar
- Ban A. Abdul Majeed
Institutions
- Hamad Medical Corporation (QA)
Publication Details
- Journal
- Molecular Genetics and Metabolism Reports
- Published
- 2025-04-11
- DOI
- https://doi.org/10.1016/j.ymgmr.2025.101217
- Primary Topic
- Folate and B Vitamins Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00