Cutaneous features in 17q21.31 deletion syndrome: A differential diagnosis for cardio-facio-cutaneous syndrome

Emma Burkitt Wright, Dian Donnai, Diana Johnson, Jill Clayton-Smith

    Research output: Contribution to journalArticlepeer-review

    Abstract

    Microdeletion of 17q21.31 causes a recurrent recognizable dysmorphic syndrome. A further four patients with 17q21.31 microdeletions are reported here in whom an earlier diagnosis of cardio-facio-cutaneous syndrome was suggested. These patients have significant similarities of facial gestalt to earlier reported 17q21.31 microdeletion patients, but a striking feature that has not been emphasized previously is the large number of naevi and other pigmentary skin abnormalities that may be present. These features, together with a coarse facial appearance, relative macrocephaly and significant learning disabilities, were what had led to the earlier diagnostic suggestion of cardio-facio-cutaneous syndrome in each of these four cases. © 2011 Wolters Kluwer Health. Lippincott Williams & Wilkins.
    Original languageEnglish
    Pages (from-to)15-20
    Number of pages5
    JournalClinical dysmorphology
    Volume20
    Issue number1
    DOIs
    Publication statusPublished - Jan 2011

    Keywords

    • 17q21.31 microdeletion syndrome
    • cardio-facio-cutaneous syndrome
    • hyperpigmentation
    • naevi

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