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The Basal Cell Naevus Syndrome: Report of a Family with Anosmia and a Case of Hypogonadotrophic Hypopituitarism
  1. D. C. Wallace*,
  2. K. J. Murphy,
  3. L. Kelly,
  4. W. H. Ward*

    Abstract

    A family with the naevoid basal cell carcinoma syndrome is described. Three affected members in one sibship suffered from anosmia. One member has shown a most severe constellation of defects including cataracts, hypertelorism, and anosmia, together with hypogonadism secondary to partial pituitary dysfunction. It is suggested that this latter also represents a previously unreported manifestation of the syndrome.

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    Footnotes

    • * From the Royal Newcastle Hospital, New South Wales, Australia.

    • From the Princess Alexandra Hospital, Brisbane, Queensland, Australia.

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