2007 Vahedi


Background and Purpose—Recently COL4A1, a gene encoding the type IV collagen a1 chain, has been found to be involved in families with autosomal-dominant porencephaly and infantile hemiparesis. In addition to neonatal stroke, some family members had experienced, during adulthood, spontaneous intracerebral hemorrhages (ICHs) and leukoencephalopathy, suggestive of underlying small-vessel disease of the brain. We now report a patient with sporadic, recurrent ICHs and a novel COL4A1 mutation.

File Download: 2007 Vahedi

Publish Date: 1 May 2007

Gould Syndrome Foundation