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Reifenstein syndrome

Wilson, J.D., Harrod, M.J., Goldstein, J.L., Hemsell, D.L. and MacDonald, P.C. (1974) Familial incomplete male pseudohermaphroditism, type 1. Evidence for androgen resistance and variable clinical manifestations in a family with the Reifenstein syndrome. The New England Journal of Medicine, 290, 1097-1103. [Pg.291]

Tager, H.S., Steiner, D.F. Peptide hormones. In Annual review of biochemistry (Snell, E.E., Boyer, P.D., Meister, A., and Richardson, C.C., eds), vol. 43, p. 509-538. Palo Alto, Calif Annual Reviews Inc. 1974 Wilson, J.D., Harrod, M.J., Goldstein, J.L., Hemsell, D.L., MacDonald, P.C. Familial incomplete male pseudohermaphroditism, type 1. Evidence for androgen resistance and variable clinical manifestations in a family with the Reifenstein syndrome. New Engl. J. Med. 290, 1097-1103 (1974)... [Pg.536]

In PAIS the degree of sexual ambiguity varies widely from individual to individual. PAIS can include other disorders, such as Reifenstein s syndrome (also known as Gilbert-Dreyfus syndrome or Lubs syndrome), which is associated with hypospadias, gynecomastia, and cryptorchism. [Pg.156]


See also in sourсe #XX -- [ Pg.3 , Pg.698 ]




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