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Article

Kallmann's syndrome: molecular pathogenesis.

The international journal of biochemistry & cell biology - 1 Aug 2003

Hu Youli, Tanriverdi Fatih, MacColl Gavin S, Bouloux Pierre-Marc G

Abstract excerpt

Kallmann's syndrome (KS) is a genetic condition characterised by hypogonadotrophic hypogonadism (HH) and anosmia; although these are the defining features of the condition, additional neurological and non-neurological sequel may also occur depending on the specific mode of inheritance. KS affects about 1 in 8000 males and 1 in 40,000 females, with most presentations being of the 'sporadic' type. Of the inherited...

Topics

Amino Acid Sequence
Animals
Extracellular Matrix Proteins
Female
Fibronectins
Heparan Sulfate Proteoglycans
Humans
Kallmann Syndrome
Male
Milk Proteins
Molecular Sequence Data

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Mutation

Nerve Tissue Proteins

Olfactory Pathways

Source

Identifiers

PMID: 12757752
DOI: 10.1016/s1357-2725(02)00395-3

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