502 - Vol. 67 /
Ed 6 /
in 2001 |
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Section: Relato de Caso |
Pages: 880 to 884 |
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Hypogonadotropic hypogonadism and anosmia: Kallmann's syndrome |
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Authors: |
Viviane Bom Schmidt 1, Renato Roithmann 2, Helena von Eye Corleta (3,4,6), Edison Capp (3,4,5) |
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Keywords: Kallmann's syndrome, hypogonadism hypogonadotrophic, anosmia
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Abstract: Kallmann's syndrome is characterized by hypogonadotrophic hypogonadism and anosmia or hyposmia. Its primary defect is an anomalous migration of the neurons responsible for the GnRH production and the neurons that compose the olfactory nerves. The syndrome affects the gonadotrophin production only, all other hypophysial hormones are normally secreted. In this paper we report and discuss two cases of Kallmann's syndrome in young women.
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Indexations: MEDLINE, Exerpta Medica, Lilacs (Index Medicus Latinoamericano), SciELO (Scientific Electronic Library Online)
CAPES: Qualis Nacional A, Qualis Internacional C
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