Becker disease: Introduction
Becker disease: A rare inherited neuromuscular disorder characterized by muscle stiffness when movement is initiated and difficulty relaxing muscles after movement had occurred. Becker disease is a recessively inherited form of myotonia congenita and usually occurs later in childhood than the dominantly inherited form and muscle stiffness is usually more severe.
More detailed information about the symptoms,
causes, and treatments of Becker disease is available below.
Symptoms of Becker disease
See full list of 10
symptoms of Becker disease
Home Diagnostic Testing
Home medical testing related to Becker disease:
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Wrongly Diagnosed with Becker disease?
Causes of Becker disease
Read more about causes of Becker disease.
Disease Topics Related To Becker disease
Research the causes of these diseases that are similar to, or related to, Becker disease:
Becker disease: Undiagnosed Conditions
Commonly undiagnosed diseases in related medical categories:
Misdiagnosis and Becker disease
Vitamin B12 deficiency under-diagnosed: The condition of Vitamin B12 deficiency
is a possible misdiagnosis of various conditions, such as multiple sclerosis (see symptoms of multiple sclerosis).
See ...read more »
Read more about Misdiagnosis and Becker disease
Becker disease: Research Doctors & Specialists
Research related physicians and medical specialists:
Other doctor, physician and specialist research services:
Evidence Based Medicine Research for Becker disease
Medical research articles related to Becker disease include:
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Becker disease: Animations
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Research about Becker disease
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Statistics for Becker disease
Becker disease: Broader Related Topics
Types of Becker disease
User Interactive Forums
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Definitions of Becker disease:
Becker disease is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Becker disease, or a subtype of Becker disease,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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