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Rare cerebrovascular anomalies in a patient with Cornelia De Lange Syndrome
BACKGROUND: Cornelia De Lange (CDL) is a rare genetic syndrome characterized by short stature, intellectual disability, skeletal abnormalities, and distinctive facial features. We present a case of CDL with several rare cerebrovascular anatomic variants that impacted the treatment of a direct cavern...
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| Publicat a: | Surg Neurol Int |
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| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Medknow Publications & Media Pvt Ltd
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4429336/ https://ncbi.nlm.nih.gov/pubmed/25984388 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/2152-7806.156772 |
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