Advances in the studies of Kallmann syndrome / 中华男科学杂志
National Journal of Andrology
; (12): 647-649, 2006.
Article
in 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.
Full text:
1
Index:
WPRIM
Main subject:
Therapeutics
/
Extracellular Matrix Proteins
/
Kallmann Syndrome
/
Rare Diseases
/
Diagnosis
/
Diagnosis, Differential
/
Receptor, Fibroblast Growth Factor, Type 1
/
Genetics
/
Nerve Tissue Proteins
Type of study:
Diagnostic_studies
/
Prognostic_studies
Limits:
Humans
/
Male
Language:
Zh
Journal:
National Journal of Andrology
Year:
2006
Type:
Article