Case series: Arterial tortuosity syndrome confirmed by homozygous SLC2A10 variants
Arterial tortuosity syndrome (ATS) is a very rare inherited connective tissue disorder caused by pathogenic variants in Solute Carrier Family 2 Member 10 (SLC2A10) gene. It primarily affects the large and medium-sized arteries, leading to abnormal elongation and tortuosity of the vascular tree. In c...
Furkejuvvon:
| Váldodahkkit: | , , , , , |
|---|---|
| Materiálatiipa: | Artigo |
| Giella: | Inglês |
| Almmustuhtton: |
Elsevier
2026-08-01
|
| Ráidu: | Radiology Case Reports |
| Fáttát: | |
| Liŋkkat: | http://www.sciencedirect.com/science/article/pii/S1930043326003596 |
| Fáddágilkorat: |
Eai fáddágilkorat, Lasit vuosttaš fáddágilkora!
|
