Literature DB >> 12029347

A probable new type of osteopenic bone disease.

Torulf L Widhe1.   

Abstract

A probable new type of osteopenic bone disease in two sisters and one female cousin is described. In infancy, the radiological findings were osteopenia, coxa vara, periosteal cloaking, bowing of the long bones, and flaring of the metaphyses. During growth, spinal pathology developed with compression of the vertebral bodies and scoliosis in one girl and kyphosis in another. All three children had genu valgum and two developed severe S-shaped bowing of the tibiae. Growth was stunted. Inheritance of this disorder is probably recessive. Type I and III collagen biosynthesis was normal. This condition is probably a hitherto undescribed form of osteogenesis imperfecta type III or a new bone disease.

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Year:  2002        PMID: 12029347     DOI: 10.1007/s00247-001-0640-0

Source DB:  PubMed          Journal:  Pediatr Radiol        ISSN: 0301-0449


  2 in total

1.  Phenotypic Spectrum in Osteogenesis Imperfecta Due to Mutations in TMEM38B: Unraveling a Complex Cellular Defect.

Authors:  Emma A Webb; Meena Balasubramanian; Nadja Fratzl-Zelman; Wayne A Cabral; Hannah Titheradge; Atif Alsaedi; Vrinda Saraff; Julie Vogt; Trevor Cole; Susan Stewart; Nicola J Crabtree; Brandi M Sargent; Sonja Gamsjaeger; Eleftherios P Paschalis; Paul Roschger; Klaus Klaushofer; Nick J Shaw; Joan C Marini; Wolfgang Högler
Journal:  J Clin Endocrinol Metab       Date:  2017-06-01       Impact factor: 5.958

Review 2.  The genetic implication of scoliosis in osteogenesis imperfecta: a review.

Authors:  Gang Liu; Jia Chen; Yangzhong Zhou; Yuzhi Zuo; Sen Liu; Weisheng Chen; Zhihong Wu; Nan Wu
Journal:  J Spine Surg       Date:  2017-12
  2 in total

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