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Seizures as an Atypical Feature of Beal’s Syndrome
Congenital contractural arachnodactyly, commonly known as Beal’s syndrome, is an extremely rare genetic disorder caused by mutations in the fibrillin-2 (FBN2) gene located on chromosome 5q23. It is an autosomal dominant inherited connective tissue disorder characterised by a Marfan-like body habitus...
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| Publicat a: | Sultan Qaboos Univ Med J |
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| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Sultan Qaboos University Medical Journal, College of Medicine & Health Sciences
2016
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4996306/ https://ncbi.nlm.nih.gov/pubmed/27606123 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18295/squmj.2016.16.03.021 |
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