
This article has more info:
http://www.dogs.net.au/sirstaffalot/page2.asp"........The present knowledge of the mode of inheritance of this disease is thought to be an autosomal irregular dominant with variable expression. Due to PHPV seldom resulting in secondary cataracts in the Stafford, those that are mildly afflicted will seldom show any form of visual impairment during the course of their lives.
Even those that are more severely afflicted, may be capable of adapting by using peripheral to compensate......"
The BVA article
http://www.bva.co.uk/public/documents/Eye_Leaflet.pdf says of this disease:
"....The mode of inheritance is complex, but the genetic data available suggest an autosomal irregular dominant gene with variable expression. The breeds examined under Schedule A are listed in the table on the right. There are currently no breeds being investigated for this condition under Schedule B......."
"...Congenital inherited ocular disease: persistent hyperplastic primary vitreous
Certified - Schedule A, Dobermann, Staffordshire Bull Terrier, Under Investigation -
Schedule B, Finnish Lapphund..."