Osteogenesis imperfecta type 2

MONDO:0008147

Osteogenesis imperfecta type II is a lethal type of osteogenesis imperfecta (OI), a genetic disorder characterized by increased bone fragility, low bone mass and susceptibility to bone fractures. Patients with type II present multiple rib and long bone fractures at birth, marked deformities, broad long bones, low density on skull X-rays, and dark sclera.

Also known as: OI type 2, OI2, Vrolik type of osteogenesis imperfecta, lethal osteogenesis imperfecta, osteogenesis imperfecta type 2, osteogenesis imperfecta type II, OI, type 2, Perinatally lethal OI

0 clinical trials for this condition and its sub-types, 0 tagged with Osteogenesis imperfecta type 2 itself.

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↑ Osteogenesis imperfecta and a reduction of bone mineral density. (308)

Including sub-types (0) Tagged with Osteogenesis imperfecta type 2 (0)

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