(vro´lik) osteogenesis imperfecta (type II), recessive form; see osteogenesis imperfecta.
Found on http://www.encyclo.co.uk/local/21001
A severe form of brittle bone disease that is characterized by short limb dwarfism, thin skin, soft skull, unusually large soft spots, blue sclerae, small nose, low nasal bridge, inguinal hernia and numerous bone fractures at birth. This extreme form is usually not compatible with life and affected babies are either stillborn or generally die duri.
Found on http://www.pregnology.com/AZ/V/3
No exact match found