Outcomes of genetic testing and prenatal diagnosis of spinal muscular atrophy in Jordan
The study highlights the importance of SMA as a clinical health problem in Jordan and demonstrates MLPA as a reliable diagnostic tool. Our findings support the integration of SMA carrier screening into national newborn screening and premarital programs to enable early diagnosis, improve genetic counseling, and facilitate gene therapy options, ultimately improving overall patient outcomes and management.
Authors
- Mohammed El‐Khateeb (ORCID: https://orcid.org/0000-0002-9675-4426)
- Rajaa Fathallah
- Mohammad Shboul (ORCID: https://orcid.org/0000-0003-3286-1422)
- Khadeeja Al‐Rashed
Institutions
- Jordan University of Science and Technology (JO)
Publication Details
- Journal
- The Journal of Maternal-Fetal & Neonatal Medicine
- Published
- 2025-08-03
- DOI
- https://doi.org/10.1080/14767058.2025.2540463
- Primary Topic
- Neurogenetic and Muscular Disorders Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Jordan University of Science and Technology