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Wiedemann‐Steiner syndrome: A case report
Wiedemann‐Steiner syndrome (WDSTS) is an exceptionally rare autosomal dominant syndrome with considerable phenotypical variation. Clinical features include dysmorphic facial and skeletal features, growth deficiency, developmental delay, hypertrichosis cubiti and various dental features. We present a...
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| Publicado no: | Clin Case Rep |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7981703/ https://ncbi.nlm.nih.gov/pubmed/33768801 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ccr3.3704 |
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