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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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| Foilsithe in: | Am J Ophthalmol Case Rep |
|---|---|
| Main Authors: | , , , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
Elsevier
2016
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| Ábhair: | |
| Rochtain Ar Líne: | 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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