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幼儿特殊面容伴发育落后与多系统畸形
Schinzel-Giedion syndrome is a rare autosomal dominant genetic disease and has the clinical features of severe delayed development, unusual facies, and multiple congenital malformations. In this case report, a 14-month-old boy had the clinical manifestations of delayed development, unusual facies (p...
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| Pubblicato in: | Zhongguo Dang Dai Er Ke Za Zhi |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
中国当代儿科杂志编辑部
2017
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7390051/ https://ncbi.nlm.nih.gov/pubmed/28774369 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7499/j.issn.1008-8830.2017.08.014 |
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