| Apert-Syndrom, Akrozephalosyndaktylie, Facies | |
| Flache Orbita, Exophthalmus, Hypertelorismus, Exotropie, Optikus Atrophie. Syndaktylie. Autosomal dominante Vererbung. | |
| Ruprecht, Klaus, Prof. Dr. med., Universitäts-Augenklinik, Homburg/Saar, Germany | |
| Q87.0 | |
| Kongenitale (angeborene) Syndrome, Mißbildungen und Anomalien (Abnormitäten) -> Hereditäre Syndrome -> Kraniostenosen -> Apert-Syndrom | |
| Kongenitale Syndrome | |
| 3888 |
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Apert-Syndrom, Akrozephalosyndaktylie, Facies-------------------------- -------------------------- -------------------------- -------------------------- -------------------------- -------------------------- -------------------------- -------------------------- -------------------------- -------------------------- -------------------------- -------------------------- |
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