GAMT Deficiency Among Pediatric Population: Clinical and Molecular Characteristics and Management.
Majdah A AlmaghrabiOsama Y MuthaffarSereen A AlahmadiMashael A AbdulsbhanMashael BamusaMaram Ahmed AljezaniSarah Y BahowarthAnas S AlyazidiWaheeb S AggadPublished in: Child neurology open (2023)
Objective: Analyze the treatment modalities used in real practice by synthesizing available literature. Methods: We reviewed and evaluated 52 cases of GAMT deficiency including 4 novel cases from Saudi Arabia diagnosed using whole-exome sequencing. All data utilized graphical presentation in the form of line charts and illustrated graphs. Results: The mean current age of was 117 months (±29.03) (range 12-372 months). The mean age of disease onset was 28.32 months (±13.68) (range 8 days - 252 months). The most prevalent symptom was developmental delays, mainly speech and motor, seizures, and intellectual disability. The male-to-female ratio was 3:1. Multiple treatments were used, with 54 pharmacological interventions, valproic acid being the most common. Creatinine monohydrate was the prevalent dietary intervention, with 25 patients reporting an improvement. Conclusion: The study suggests that efficient treatment with appropriate dietary intervention can improve patients' health, stressing that personalized treatment programs are essential in managing this disorder.
Keyphrases
- end stage renal disease
- intellectual disability
- randomized controlled trial
- ejection fraction
- healthcare
- chronic kidney disease
- saudi arabia
- public health
- autism spectrum disorder
- peritoneal dialysis
- systematic review
- prognostic factors
- mental health
- replacement therapy
- physical activity
- single molecule
- quality improvement
- risk assessment