Klinefelter's syndrome associated with a D/D translocation.

AUTOR(ES)

Sparagana, M

RESUMO

A case of Klinefelter's syndrome and a simultaneous familial D/D translocation is described. The clinical, endocrine, and psychiatric features were typical of those found in Klinefelter's syndrome. Other family members showed no obvious abnormality despite presence of the D/D translocation.

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