載入...
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...
Na minha lista:
| 發表在: | Adv Biomed Res |
|---|---|
| Main Authors: | , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Medknow Publications & Media Pvt Ltd
2015
|
| 主題: | |
| 在線閱讀: | 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 |
| 標簽: |
添加標簽
沒有標簽, 成為第一個標記此記錄!
|