Naumoff short-rib polydactyly syndrome compounded with Mohr oral-facial-digital syndrome

L. W. Young, L. L. Wilhelm, Craig W. Zuppan, Robin Clark

    Research output: Contribution to journalArticlepeer-review

    Abstract

    A stillborn baby boy had findings of severe constitutional dwarfism with short limbs, short ribs, and polydactyly that were consistent with Naumoff (type III) short-rib polydactyly syndrome. He also had additional congenital anomalies, including cleft palate, notching of the upper lip, small tongue with accessory sublingual tissue. These oral and pharyngeal anomalies were consistent with Mohr (type II) oral-facial-digital syndrome. We suggest the stillborn infant represented a compound of Naumoff short-rib polydactyly syndrome (SRPS-III) and Mohr oral-facial-digital syndrome (OFDS-II).

    Original languageEnglish
    Pages (from-to)31-35
    Number of pages5
    JournalPediatric Radiology
    Volume31
    Issue number1
    DOIs
    StatePublished - 2001

    ASJC Scopus Subject Areas

    • Pediatrics, Perinatology, and Child Health
    • Radiology Nuclear Medicine and imaging

    Keywords

    • Orofaciodigital Syndromes/complications
    • Humans
    • Fatal Outcome
    • Male
    • Short Rib-Polydactyly Syndrome/complications
    • Infant, Newborn

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