Advances in the studies of Kallmann syndrome / 中华男科学杂志
National Journal of Andrology
; (12): 647-649, 2006.
Article
em Zh
| WPRIM
| ID: wpr-343551
Biblioteca responsável:
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.
Texto completo:
1
Índice:
WPRIM
Assunto principal:
Terapêutica
/
Proteínas da Matriz Extracelular
/
Síndrome de Kallmann
/
Doenças Raras
/
Diagnóstico
/
Diagnóstico Diferencial
/
Receptor Tipo 1 de Fator de Crescimento de Fibroblastos
/
Genética
/
Proteínas do Tecido Nervoso
Tipo de estudo:
Diagnostic_studies
/
Prognostic_studies
Limite:
Humans
/
Male
Idioma:
Zh
Revista:
National Journal of Andrology
Ano de publicação:
2006
Tipo de documento:
Article