The trichorhinophalangeal dysplasia syndrome: Report of eight kindreds, with emphasis on hip complications, late presentations, and premature osteoarthrosis

Ray Cope, Rodney K. Beals, Robert (Rob) Bennett

    Research output: Contribution to journalArticle

    11 Citations (Scopus)

    Abstract

    The trichorhinophalangeal dysplasia syndrome is characterized by peripheral cone-shaped epiphyses and unusual facies and hair. It is generally considered to be an uncommon dysplasia that presents in childhood. Thirteen cases in eight kindreds are reported. In four patients, the diagnosis was not established until after the 40th year, and it is suggested that the dysplasia may present in adult life and be more common than is generally appreciated. The skeletal stigmata of the syndrome are described, with special reference to hip involvement, and a severe and progressive degenerative arthritis is reported.

    Original languageEnglish (US)
    Pages (from-to)133-138
    Number of pages6
    JournalJournal of Pediatric Orthopaedics
    Volume6
    Issue number2
    StatePublished - 1986

    Fingerprint

    Osteoarthritis
    Hip
    Christianity
    Epiphyses
    Hair

    Keywords

    • Degenerative arthritis
    • Dysplasia
    • Heredity
    • Hip complications
    • Trichorhinophalangeal dysplasia syndrome

    ASJC Scopus subject areas

    • Orthopedics and Sports Medicine
    • Pediatrics, Perinatology, and Child Health
    • Surgery

    Cite this

    The trichorhinophalangeal dysplasia syndrome : Report of eight kindreds, with emphasis on hip complications, late presentations, and premature osteoarthrosis. / Cope, Ray; Beals, Rodney K.; Bennett, Robert (Rob).

    In: Journal of Pediatric Orthopaedics, Vol. 6, No. 2, 1986, p. 133-138.

    Research output: Contribution to journalArticle

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