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Dentinogenesis imperfecta

Eastoe, J. E., Martens, P., Thomas, N. R. The amino acid composition of human hard tissue collagens in osteogenesis imperfecta and dentinogenesis imperfecta. Calc. Tiss. Res. 12, 91 (1973)... [Pg.127]

I Normal stature little or no deformity blue sclerae hearing loss in 50% of individuals dentinogenesis imperfecta rare but may distinguish a subset AD... [Pg.31]

III Progressively deforming bones, usually with moderate deformity at birth extreme short stature sclerae variable in hue, often lighten with age common dentinogenesis imperfecta and hearing loss AD with parental mosaicism autosomal recessive (rare)... [Pg.31]

IV Mild-to-moderate bone deformity variable short stature white or blue sclerae common dentinogenesis imperfecta hearing loss in some patients AD with parental mosaicism... [Pg.31]

V Bone fragility mild-to-moderate short stature no dentinogenesis imperfecta radioulnar synostosis hyperplastic callus formation Probably AD... [Pg.31]

Type I collagen mutations associated with osteogenesis imperfecta Dentinogenesis imperfecta type I (see also Chap. 9) Opalescent blue-gray or yellow-brown teeth because of abnormal dentin calcification... [Pg.105]

Dentin sialophosphoprotein (DSPP), a glycoprotein of the connective tissue stroma (Chap. 9) Dentinogenesis imperfecta type II Changes resemble type I dentinogenesis imperfecta (Chap. 9)... [Pg.105]

See other pages where Dentinogenesis imperfecta is mentioned: [Pg.480]    [Pg.32]    [Pg.32]    [Pg.33]    [Pg.106]    [Pg.143]    [Pg.241]    [Pg.241]    [Pg.241]    [Pg.339]    [Pg.325]    [Pg.660]    [Pg.296]    [Pg.480]    [Pg.32]    [Pg.32]    [Pg.33]    [Pg.106]    [Pg.143]    [Pg.241]    [Pg.241]    [Pg.241]    [Pg.339]    [Pg.325]    [Pg.660]    [Pg.296]   
See also in sourсe #XX -- [ Pg.325 ]



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Dentinogenesis

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