Kallmann Syndrome: Introduction
Kallmann Syndrome: A rare inherited condition characterized by hypogonadism, eunuchoidism and impaired or absent sense of smell. The condition occurs as a result of failure of a part of the hypothalamus which results in hormonal imbalance.
More detailed information about the symptoms,
causes, and treatments of Kallmann Syndrome is available below.
Symptoms of Kallmann Syndrome
See full list of 10
symptoms of Kallmann Syndrome
Home Diagnostic Testing
Home medical testing related to Kallmann Syndrome:
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Wrongly Diagnosed with Kallmann Syndrome?
Kallmann Syndrome: Related Patient Stories
Kallmann Syndrome: Complications
Read more about complications of Kallmann Syndrome.
Causes of Kallmann Syndrome
Read more about causes of Kallmann Syndrome.
More information about causes of Kallmann Syndrome:
Disease Topics Related To Kallmann Syndrome
Research the causes of these diseases that are similar to, or related to, Kallmann Syndrome:
Kallmann Syndrome: Undiagnosed Conditions
Commonly undiagnosed diseases in related medical categories:
Misdiagnosis and Kallmann Syndrome
Misdiagnosed weight-related causes of infertility: A woman's weight status
can affect her level of fertility.
Although obesity or overweight can in themselves reduce...read more »
Read more about Misdiagnosis and Kallmann Syndrome
Kallmann Syndrome: Research Doctors & Specialists
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Kallmann Syndrome: Rare Types
Rare types of diseases and disorders in related medical categories:
Evidence Based Medicine Research for Kallmann Syndrome
Medical research articles related to Kallmann Syndrome include:
Click here to find more evidence-based articles on the TRIP Database
Kallmann Syndrome: Animations
More Kallmann Syndrome animations & videos
Research about Kallmann Syndrome
Visit our research pages for current research about Kallmann Syndrome treatments.
Clinical Trials for Kallmann Syndrome
The US based website ClinicalTrials.gov lists information on both federally
and privately supported clinical trials using human volunteers.
Some of the clinical trials listed on ClinicalTrials.gov for Kallmann Syndrome include:
Read more about Clinical Trials for Kallmann Syndrome
Statistics for Kallmann Syndrome
Kallmann Syndrome: Broader Related Topics
Types of Kallmann Syndrome
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Definitions of Kallmann Syndrome:
A syndrome, sometimes considered as three separate entities (Kalmann syndromes 1, 2, and 3), characterized mainly by reduced hypothalamic function and reduced pituitary gonadotropic activity and deficiency of gonadotropin-releasing hormone with resulting hypogonadism and absent or reduced sense of smell due to agenesis of the olfactory bulbs. Associated anomalies include cleft palate, neurosensory hearing loss, congenital heart defect, intestinal malrotation, renal agenesis, hypertension, mental retardation, color blindness, and other defects. Most abnormalities occur in types 1 and 2; type 3 is marked mainly by hypogonadotropic hypogonadism, anosmia, and craniofacial abnormalities.
- (Source - Diseases Database)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Kallmann Syndrome as a "rare disease".
Source - Orphanet
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