Structural brain abnormalities in Pallister-Killian syndrome: a neuroimaging study of 31 children
Abstract Background Pallister-Killian syndrome (PKS) is a rare genetic disorder caused by mosaic tetrasomy of 12p with wide neurological involvement. Intellectual disability, developmental delay, behavioral problems, epilepsy, sleep disturbances, and brain malformations have been described in most i...
Furkejuvvon:
| Váldodahkkit: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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| Materiálatiipa: | Artigo |
| Giella: | Inglês |
| Almmustuhtton: |
BMC
2024-03-01
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| Ráidu: | Orphanet Journal of Rare Diseases |
| Liŋkkat: | https://doi.org/10.1186/s13023-024-03065-5 |
| Fáddágilkorat: |
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