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Craniofacial Abnormalities in Hutchinson-Gilford Progeria Syndrome
HGPS is a rare syndrome of segmental premature aging. Our goal was to expand the scope of structural bone and soft-tissue craniofacial abnormalities in HGPS through CT or MR imaging. Using The Progeria Research Foundation Medical and Research Database, 98 imaging studies on 25 patients, birth to 14....
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| Gepubliceerd in: | AJNR Am J Neuroradiol |
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| Hoofdauteurs: | , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
American Society of Neuroradiology
2012
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7966543/ https://ncbi.nlm.nih.gov/pubmed/22460337 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3174/ajnr.A3088 |
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