osteogenesis imperfecta type II

[MIM*166210]

a perinatal lethal form associated with stillbirth or lifespan less than 1 year; very fragile connective tissue, and radiographic findings of in utero fractures, large soft cranium, micromelia, tubular long bones, and beaded ribs.

os·te·o·gen·e·sis im·per·fec·ta type II

(os'tē-ō-jen'ĕ-sis im'pĕr-fek'tă tīp)

A perinatal lethal form associated with stillbirth or lifespan less than 1 year; very fragile connective tissue, and radiographic findings of fractures in utero, large soft cranium, micromelia, tubular long bones, and beaded ribs.

os·te·o·gen·e·sis im·per·fec·ta type II

(os'tē-ō-jen'ĕ-sis im-pĕr-fek'tă tīp) [MIM*166210]

Perinatal lethal form associated with stillbirth or lifespan less than 1 year.

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References in periodicals archive ?

Osteogenesis imperfecta type II delineation of the phenotype with reference to genetic heterogeneity.

Osteogenesis imperfecta in adult twins responded to treatment with pamidronate/Osteogenezis imperfektali eriskin ikizlerin pamidronat tedavisine olumlu cevabi