Kallmann syndrome, type 3, recessive
Kallmann syndrome, type 3, recessive: Introduction
Kallmann syndrome, type 3, recessive: A rare inherited condition characterized by hypogonadism 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. Type 3 is recessively inherited and the genetic defect is located at chromosome 20p13.
More detailed information about the symptoms,
causes, and treatments of Kallmann syndrome, type 3, recessive is available below.
Symptoms of Kallmann syndrome, type 3, recessive
See full list of 7
symptoms of Kallmann syndrome, type 3, recessive
Home Diagnostic Testing
Home medical testing related to Kallmann syndrome, type 3, recessive:
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Wrongly Diagnosed with Kallmann syndrome, type 3, recessive?
Kallmann syndrome, type 3, recessive: Complications
Review possible medical complications related to Kallmann syndrome, type 3, recessive:
Causes of Kallmann syndrome, type 3, recessive
Read more about causes of Kallmann syndrome, type 3, recessive.
Less Common Symptoms of Kallmann syndrome, type 3, recessive
Read more about symptoms of Kallmann syndrome, type 3, recessive
Kallmann syndrome, type 3, recessive: Undiagnosed Conditions
Commonly undiagnosed diseases in related medical categories:
Misdiagnosis and Kallmann syndrome, type 3, recessive
Misdiagnosed weight-related causes of infertility: A woman's weight status
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Kallmann syndrome, type 3, recessive: Research Doctors & Specialists
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Other doctor, physician and specialist research services:
Kallmann syndrome, type 3, recessive: Rare Types
Rare types of diseases and disorders in related medical categories:
Kallmann syndrome, type 3, recessive: Animations
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Statistics for Kallmann syndrome, type 3, recessive
Kallmann syndrome, type 3, recessive: Broader Related Topics
Types of Kallmann syndrome, type 3, recessive
User Interactive Forums
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Definitions of Kallmann syndrome, type 3, recessive:
Kallmann syndrome, type 3, recessive is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Kallmann syndrome, type 3, recessive, or a subtype of Kallmann syndrome, type 3, recessive,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Contents for Kallmann syndrome, type 3, recessive:
- Kallmann syndrome, type 3, recessive
- What is Kallmann syndrome, type 3, recessive?
- Prevalence and Incidence of Kallmann syndrome, type 3, recessive
- Videos related to Kallmann syndrome, type 3, recessive
- Types of Kallmann syndrome, type 3, recessive
- Causes of Kallmann syndrome, type 3, recessive
- Symptoms of Kallmann syndrome, type 3, recessive
- Diagnostic Tests for Kallmann syndrome, type 3, recessive
- Home Testing and Kallmann syndrome, type 3, recessive
- Signs of Kallmann syndrome, type 3, recessive
- Complications of Kallmann syndrome, type 3, recessive
- Misdiagnosis of Kallmann syndrome, type 3, recessive
- Undiagnosed Kallmann syndrome, type 3, recessive
- Treatments for Kallmann syndrome, type 3, recessive
- Doctors and Medical Specialists for Kallmann syndrome, type 3, recessive
- Statistics about Kallmann syndrome, type 3, recessive
- Glossary for Kallmann syndrome, type 3, recessive