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Ophthalmic considerations in patients with Pfeiffer syndrome
PURPOSE: We report here a newborn male infant with striking features consistent with severe Pfeiffer syndrome type II, including cloverleaf skull deformity with pansynostosis, extreme proptosis, upper extremity contractures, broad big toes and thumbs with varus deviation and genetic mutation in the...
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| Veröffentlicht in: | Am J Ophthalmol Case Rep |
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| Hauptverfasser: | , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Elsevier
2016
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5757361/ https://ncbi.nlm.nih.gov/pubmed/29503887 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajoc.2016.04.001 |
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