Display Settings:

Format

Send to:

Choose Destination
    Am J Hum Genet. 2010 Jul 9;87(1):110-4. Epub 2010 Jun 24.

    Identification of a frameshift mutation in Osterix in a patient with recessive osteogenesis imperfecta.

    Source

    CIBER de enfermedades Raras, 28046 Madrid, Spain.

    Abstract

    Osteogenesis imperfecta, or "brittle bone disease," is a type I collagen-related condition associated with osteoporosis and increased risk of bone fractures. Using a combination of homozygosity mapping and candidate gene approach, we have identified a homozygous single base pair deletion (c.1052delA) in SP7/Osterix (OSX) in an Egyptian child with recessive osteogenesis imperfecta. The clinical findings from this patient include recurrent fractures, mild bone deformities, delayed tooth eruption, normal hearing, and white sclera. OSX encodes a transcription factor containing three Cys2-His2 zinc-finger DNA-binding domains at its C terminus, which, in mice, has been shown to be essential for bone formation. The frameshift caused by the c.1052delA deletion removes the last 81 amino acids of the protein, including the third zinc-finger motif. This finding adds another locus to the spectrum of genes associated with osteogenesis imperfecta and reveals that SP7/OSX also plays a key role in human bone development.

    Copyright 2010 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved.

    PMID:
    20579626
    [PubMed - indexed for MEDLINE]
    PMCID: PMC2896769
    Free PMC Article

    Images from this publication.See all images (2) Free text

    Figure 1
    Figure 2

      Supplemental Content

      Click here to read Click here to read

      Recent activity

      Your browsing activity is empty.

      Activity recording is turned off.

      Turn recording back on

      See more...
      Write to the Help Desk