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Published on: July 30, 2014
Metaphyseal dysplasia, Spahr type; missense MMP13 mutations in two Iraqi siblings
Shereen Tadros1, Richard H Scott, Alistair D Calder
1aNorth East Thames Regional Genetics Service bDepartment of Radiology, Great Ormond Street Hospital for Children, London, UK.
Abstract:
We report on two siblings of Iraqi descent with clinical and radiographic features of metaphyseal dysplasia, Spahr type (MDST), born to consanguineous unaffected parents. Molecular testing confirmed pathogenic mutations in MMP13. We review the considerable overlap between MDST and other related disorders. These cases confirm the phenotypic variability and regressive nature of MDST in addition to suggesting bone fragility as a feature.
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