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Hutchinson–Gilford progeria syndrome with severe calcific aortic valve stenosis
Hutchinson–Gilford progeria syndrome (HGPS) is a rare premature aging syndrome that results from mutation in the Laminin A gene. This case report of a 12-year-old girl with HGPS is presented for the rarity of the syndrome and the classical clinical features that were observed in the patient. All pat...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medknow Publications
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3180988/ https://ncbi.nlm.nih.gov/pubmed/21976890 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0974-2069.84670 |
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