Advances in the studies of Kallmann syndrome / 中华男科学杂志
National Journal of Andrology
; (12): 647-649, 2006.
Article
de Zh
| WPRIM
| ID: wpr-343551
Bibliothèque responsable:
WPRO
ABSTRACT
Kallmann syndrome (KS) is a rare hereditary disease. It is characterized by hypogonadotrophic hypogonadism in association with anosmia or hyposmia. At present, three modes of inheritance and genes related to KS have been identified. This review focuses on the clinical diagnosis and advances in the studies of the pathogenesis gene for Kallmann syndrome.
Texte intégral:
1
Indice:
WPRIM
Sujet Principal:
Thérapeutique
/
Protéines de la matrice extracellulaire
/
Syndrome de Kallmann
/
Maladies rares
/
Diagnostic
/
Diagnostic différentiel
/
Récepteur FGFR1
/
Génétique
/
Protéines de tissu nerveux
Type d'étude:
Diagnostic_studies
/
Prognostic_studies
Limites du sujet:
Humans
/
Male
langue:
Zh
Texte intégral:
National Journal of Andrology
Année:
2006
Type:
Article