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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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References

    1. J Ment Defic Res. 1965 Jun;9:125-30 - PubMed
    1. Acta Med Scand. 1962 Jan;171:13-21 - PubMed
    1. Radiology. 1972 Jul;104(1):1-11 - PubMed
    1. J Ment Defic Res. 1974 Dec;18(4):317-25 - PubMed
    1. J Clin Endocrinol Metab. 1976 Aug;43(2):400-11 - PubMed

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