Unprecedented report: First female monozygotic twins as carriers of Hutchinson-Gilford progeria syndrome
Hutchinson-Gilford Progeria Syndrome (HGPS) is a rare genetic condition characterized by premature aging resulting from an autosomal mutation in the LMNA gene. This article presents a groundbreaking instance of the first female monozygotic twins affected by HGPS, originating from Brazil, highlighti...
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| Autors principals: | , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Aydın Pediatric Society
2024-06-01
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| Col·lecció: | Trends in Pediatrics |
| Matèries: | |
| Accés en línia: | https://trendspediatrics.com/article/view/115 |
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