VLDLR-associated cerebellar hypoplasia (VLDLRCH) is a rare autosomal recessive condition caused by a disruption of the VLDLR gene.
[1][2] First described as a form of cerebral palsy in the 1970s,[3] it is associated with parental consanguinity and is found in secluded communities, with a number of cases described in Hutterite families.
[4] This genetic disorder article is a stub.
You can help Wikipedia by expanding it.