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Novel ANKH mutation in a patient with sporadic craniometaphyseal dysplasia

Authors

  • Allison Zajac,

    1. Division of Plastic and Reconstructive Surgery, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania
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  • Seung-Hak Baek,

    1. Department of Orthodontics, Seoul National University, Seoul, South Korea
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  • Imad Salhab,

    1. Division of Plastic and Reconstructive Surgery, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania
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  • Melissa A. Radecki,

    1. Division of Plastic and Reconstructive Surgery, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania
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  • Sukwha Kim,

    1. Department of Reconstructive Plastic Surgery, Seoul National University, Seoul, South Korea
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  • Hakon Hakonarson,

    1. Center for Applied Genomics and Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania
    2. Department of Paediatrics, University of Pennsylvania School of Medicine, Philadelphia, PA
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  • Hyun-Duck Nah

    Corresponding author
    1. Division of Plastic and Reconstructive Surgery, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania
    2. Division of Plastic Surgery, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania
    • 1116G/ARC, 3615 Civic Center Blvd, The Children's Hospital of Philadelphia, Philadelphia, PA 19104.
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  • How to cite this article: Zajac A, Baek S-H, Salhab I, Radecki MA, Kim S, Hakonarson H, Nah H-D. 2010. Novel ANKH mutation in a patient with sporadic craniometaphyseal dysplasia. Am J Med Genet Part A 152A:770–776.

Abstract

Craniometaphyseal dysplasia is caused by mutations in ANKH (ankylosis, progressive homolog [mouse]) in the majority of cases, and all of the reported mutations are single amino acid changes. Genomic DNA from an affected patient, his biological parents, and a sibling was amplified and ANKH was sequenced. The affected patient had a complex heterozygous mutation in exon 7 (c.936T > C, c.938C > G, c.942_953delTGGTTGACGGAA), predicting p.Try290Gln and p.Trp292_Glu295del. We studied the effect of the predicted mutation on the subcellular distribution of ANKH protein. Immunofluorescent labeling of COS-7 cells transduced with normal or mutant Ank (murine progressive ankylosis), showed that normal Ank localized to both the plasma membrane and cytoplasm, whereas mutant Ank was detected only in the cytoplasmic compartment. We propose that this craniometaphyseal dysplasia mutation causes a loss of ANKH protein expression and activity in the plasma membrane as a result of aberrant intracellular protein trafficking. © 2010 Wiley-Liss, Inc.

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