Case 48: Osteogenesis Imperfecta of the Temporal Bone

Author:

Heimert Tamra L.,Lin Doris D. M.,Yousem David M.

Publisher

Radiological Society of North America (RSNA)

Subject

Radiology, Nuclear Medicine and imaging

Reference21 articles.

1. Osteogenesis Imperfecta

2. Mutations in fibrillar collagens (types I, II, III, and XI), fibril-associated collagen (type IX), and network-forming collagen (type X) cause a spectrum of diseases of bone, cartilage, and blood vessels

3. Ablin DS.Osteogenesis imperfecta: a review.Can Assoc Radiol J1998; 49:110-123.

4. Sykes B, Ogilvie D, Wordsworth P, Anderson , Jones N.Osteogenesis imperfecta is linked to both type I collagen structural genes.Lancet1986; 2:69-72.

5. Sykes B, Ogilvie D, Wordsworth P, et al.Consistent linkage of dominantly inherited osteogenesis imperfecta to the type I collagen loci: COL1A1 and COL1A2.Am J Hum Genet1990; 46:293-307.

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