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Case Reports
. 1978 Feb;15(1):63-6.
doi: 10.1136/jmg.15.1.63.

Primary hypogonadism in the Borjeson-Forssman-Lehmann syndrome

F T Weber, J L Frias, R L Julius, A H Felman
Case Reports

Primary hypogonadism in the Borjeson-Forssman-Lehmann syndrome

F T Weber et al. J Med Genet. 1978 Feb.

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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