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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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| Publicat a: | Clin Case Rep |
|---|---|
| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
John Wiley and Sons Inc.
2021
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| Matèries: | |
| Accés en línia: | 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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