Harvard Catalyst Profiles

Contact, publication, and social network information about Harvard faculty and fellows.

Kallmann Syndrome

"Kallmann Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

A genetically heterogeneous disorder caused by hypothalamic GNRH deficiency and OLFACTORY NERVE defects. It is characterized by congenital HYPOGONADOTROPIC HYPOGONADISM and ANOSMIA, possibly with additional midline defects. It can be transmitted as an X-linked (GENETIC DISEASES, X-LINKED), an autosomal dominant, or an autosomal recessive trait.


This graph shows the total number of publications written about "Kallmann Syndrome" by people in Harvard Catalyst Profiles by year, and whether "Kallmann Syndrome" was a major or minor topic of these publication.
Bar chart showing 55 publications over 23 distinct years, with a maximum of 6 publications in 2008 and 2010
To see the data from this visualization as text, click here.
Related Networks
People
Explore
_
Similar Concepts
_
Top Journals 
_
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.