The Patterson syndrome, leprechaunism, and pseudoleprechaunism

T. J. David, B. W. Webb, I. R S Gordon

    Research output: Contribution to journalArticlepeer-review

    Abstract

    A bizzare syndrome has hitherto masqueraded as leprechaunism, and although it is a quite different disorder it has been used as the prototype of leprechaunism in some birth defects atlases. It is proposed that this condition is designated the Patterson syndrome and details of a second case are reported. The features of this connective tissue and neuroendocrine disorder include bronzed hyperpigmentation, cutis laxa of the hands and feet, bodily disproportion, severe mental retardation, and major bony deformities. Radio-graphs revealed a unique and gross generalised skeletal dysplasia, unlikely to be confused with any other disorder. The endocrine abnormality comprised hyperadrenocorticism, cushingoid features, and diabetes mellitus in the first case, and premature adrenarche in the second case. The pathogenesis and aetiology of the Patterson syndrome are unknown, although quantitative and qualitative abnormalities of mucopolysaccharide excretion were found in the second case.
    Original languageEnglish
    Pages (from-to)294-298
    Number of pages4
    JournalJournal of Medical Genetics
    Volume18
    Issue number4
    Publication statusPublished - 1981

    Fingerprint

    Dive into the research topics of 'The Patterson syndrome, leprechaunism, and pseudoleprechaunism'. Together they form a unique fingerprint.

    Cite this