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Title: Primary hypogonadism in the Borjeson-Forssman-Lehmann syndrome. Author: Weber FT, Frias JL, Julius RL, Felman AH. Journal: J Med Genet; 1978 Feb; 15(1):63-6. PubMed ID: 564968. 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.[Abstract] [Full Text] [Related] [New Search]