Zusammenfassung
Die primäre vitreoretinale Dysplasie ist ein sehr seltener, genetisch heterogener Befund. Er kommt bei Chromosomenaberrationen vor, speziell Trisomie 13, aber auch im Rahmen verschiedener Syndrome mit auto- oder gonosomalen Erbgang [11, 12, 4, 14].
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© 1992 Springer-Verlag Berlin Heidelberg
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Oexle, K., Bentele, K., Meinecke, R., Dannheim, F. (1992). Computertomographischer Retinoblastomverdacht beim Neugeborenen mit familiärer vitreoretinaler Dysplasie. In: Köhler, B., Keimer, R. (eds) Aktuelle Neuropädiatrie 1991. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-77129-3_101
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