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The Schwartz-Jampel syndrome: Case report and review of literature
Schwartz-Jampel syndrome (SJS), first described in the United States in 1962, is a hereditary disorder characterized by facial dysmorphism and muscle stiffness. We describe the first case of a Persian 9-year-old boy with SJS and review the literature. The child had a short neck, blepharophimosis, fl...
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| Publicado en: | Adv Biomed Res |
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| Autores principales: | , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Medknow Publications & Media Pvt Ltd
2015
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4581134/ https://ncbi.nlm.nih.gov/pubmed/26436077 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/2277-9175.162538 |
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