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Pallister–Killian syndrome in a two‐year‐old boy
Pallister–Killian syndrome (PKS) is a rare, sporadic, multisystem developmental disorder characterized by craniofacial dysmorphic features. We report a case of a two‐year‐old boy with PKS to highlight the cutaneous findings and emphasize the importance of diagnostic skin biopsies in patients with cu...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2017
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5457980/ https://www.ncbi.nlm.nih.gov/pubmed/28588808 http://dx.doi.org/10.1002/ccr3.892 |