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Crouzon Syndrome in a Ten-week-old Infant: A Case Report
Crouzon syndrome is a rare genetic disorder. We report a rare case of Crouzon syndrome in a very young infant with distinct features of craniofacial malformations. A 10-week-old male child presented with features of craniofacial dysostosis with abnormal shape of the skull, proptosis, hypertelorism,...
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| Publicado en: | Saudi J Med Med Sci |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Wolters Kluwer - Medknow
2020
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7305672/ https://ncbi.nlm.nih.gov/pubmed/32587497 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/sjmms.sjmms_38_19 |
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