Advances in the studies of Kallmann syndrome / 中华男科学杂志
National Journal of Andrology
; (12): 647-649, 2006.
Article
在 Zh
| WPRIM
| ID: wpr-343551
Responsible library:
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.
全文:
1
索引:
WPRIM
主要主题:
Therapeutics
/
Extracellular Matrix Proteins
/
Kallmann Syndrome
/
Rare Diseases
/
Diagnosis
/
Diagnosis, Differential
/
Receptor, Fibroblast Growth Factor, Type 1
/
Genetics
/
Nerve Tissue Proteins
研究类型:
Diagnostic_studies
/
Prognostic_studies
限制:
Humans
/
Male
语言:
Zh
期刊:
National Journal of Andrology
年:
2006
类型:
Article