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Primary hypogonadism in the Borjeson-Forssman-Lehmann syndrome.
  1. F T Weber,
  2. J L Frias,
  3. R L Julius,
  4. A H Felman

    Abstract

    A 28-year-old man with mental retardation and multiple congenital malformations was found to have the classical features of Borjeson-Forssman-Lehmann syndrome. Endocrine evaluations showed primary hypogonadism as the underlying endocrine abnormality rather than hypopituitarism as suggested in earlier reports.

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