Knobloch syndrome
Description
A rare systemic disorder characterized by vitreoretinal and macular degeneration, as well as occipital encephalocele.
Cell Lines
Link
For more information, please consult the corresponding entry in Orphanet* .
*Orphanet: an online rare disease and orphan drug data base. Copyright, INSERM 1999. Available on http://www.orpha.net.