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Primary hypogonadism in the Borjeson-Forssman-Lehmann syndrome.

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 earlie...

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Dettagli Bibliografici
Autori principali: Weber, F T, Frias, J L, Julius, R L, Felman, A H
Natura: Artigo
Lingua:Inglês
Pubblicazione: 1978
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC1012825/
https://ncbi.nlm.nih.gov/pubmed/564968
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