Kallmann syndrome, type 1, X-linked

Common Name(s)

Kallmann syndrome, type 1, X-linked, Kallmann syndrome 1

Kallmann syndrome 1 is an inherited disorder characterized by delayed or absent puberty and an impaired sense of smell. Other symptoms may include color blindness, cleft lip or palate, abnormal eye movements, hearing loss, failure of one of the kidneys to develop, mirror image hand movements, abnormalities of tooth development, and infertility. This disorder is a form of hypogonadotropic hypogonadism. Affected males are usually born with a small penis and undescended testicles. Affected females usually do not begin menstruating at puberty and have little or no breast development.  Kallmann syndrome 1 is the most common type of Kallmann syndrome (there are four types identified at this time). It is caused by mutations in the KAL1 gene and is inherited in an X-linked recessive fashion.   
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Kallmann syndrome, type 1, X-linked" for support, advocacy or research.

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Scientific Literature

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Clinical Trial Information This information is provided by ClinicalTrials.gov

A Phase I/II Study of Betalutin for Treatment of Relapsed Non-Hodgkin Lymphoma
 

Status: Recruiting

Condition Summary: Non-Hodgkin Lymphoma

 

Last Updated: 19 Feb 2013

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