In vivo structural neuroimaging evaluation of the hypothalamus in Prader-Willi Syndrome sub-genotypes
Abstract Purpose Prader-Willi Syndrome (PWS) is a rare genetic disorder with a heterogeneous phenotype, caused by loss of expression of genes on the paternally inherited chromosome 15q11.2-15q13.3, primarily due to paternal deletion of these genes. PWS with paternal deletion can be categorised into...
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| Автори: | , , , , , , |
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| Формат: | Artigo |
| Мова: | Inglês |
| Опубліковано: |
Springer
2026-04-01
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| Серія: | Journal of Rare Diseases |
| Предмети: | |
| Онлайн доступ: | https://doi.org/10.1007/s44162-026-00173-7 |
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