A look at Loeys Dietz syndrome with an autopsy case: a case report and literature review
Abstract Background Loeys Dietz Syndrome (LDS) is a rare autosomal dominant genetic disease that was identified in 2005. The disease occurs with the mutation of the genes encoding the receptors and ligands of Transforming Growth Factor Beta. It progresses with skeletal system, cardiovascular, cranio...
Guardado en:
| Autores principales: | , , , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Springer
2025-12-01
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| Colección: | Journal of Rare Diseases |
| Materias: | |
| Acceso en línea: | https://doi.org/10.1007/s44162-025-00139-1 |
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