Myotonic Dystrophy: Introduction
Myotonic dystrophy is an inherited disorder in which the muscles contract but have decreasing power to relax. With this condition, the muscles also ... more about Myotonic Dystrophy.
Myotonic Dystrophy: An inherited disorder characterized by progressive muscle weakness and wasting as well as eye defects, heart abnormalities and other anomalies. The severity of the condition is greatly variable. There are two type of myotonic dystrophy with type 1 being more severe than type 2.
More detailed information about the symptoms,
causes, and treatments of Myotonic Dystrophy is available below.
Symptoms of Myotonic Dystrophy
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symptoms of Myotonic Dystrophy
Treatments for Myotonic Dystrophy
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Wrongly Diagnosed with Myotonic Dystrophy?
Myotonic Dystrophy: Related Patient Stories
Myotonic Dystrophy: Deaths
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Myotonic Dystrophy: Complications
Read more about complications of Myotonic Dystrophy.
Causes of Myotonic Dystrophy
Read more about causes of Myotonic Dystrophy.
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Disease Topics Related To Myotonic Dystrophy
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Evidence Based Medicine Research for Myotonic Dystrophy
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Myotonic Dystrophy: Animations
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Prognosis for Myotonic Dystrophy
Prognosis for Myotonic Dystrophy:
non-progressive condition which may improve with age
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Research about Myotonic Dystrophy
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Clinical Trials for Myotonic Dystrophy
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 Myotonic Dystrophy include:
See full list of 6
Clinical Trials for Myotonic Dystrophy
Statistics for Myotonic Dystrophy
Myotonic Dystrophy: Broader Related Topics
Types of Myotonic Dystrophy
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Article Excerpts about Myotonic Dystrophy
Myotonic dystrophy is an inherited disorder in which the muscles contract but have decreasing power to relax. With this condition, the muscles also become weak and waste away.
(Source: Genes and Disease by the National Center for Biotechnology)
Definitions of Myotonic Dystrophy:
An autosomal dominant neuromuscular disorder which usually presents in early adulthood, characterized by progressive muscular atrophy (most frequently involving the hands, forearms, and face), myotonia, frontal baldness, lenticular opacities, and testicular atrophy. Cardiac conduction abnormalities, diaphragmatic weakness, and mild mental retardation may also occur. Congenital myotonic dystrophy is a severe form of this disorder, characterized by neonatal MUSCLE HYPOTONIA, feeding difficulties, respiratory muscle weakness, and an increased incidence of MENTAL RETARDATION. (From Adams et al., Principles of Neurology, 6th ed, pp1423-5; Joynt, Clinical Neurology, 1997, Ch16, pp16-7)
- (Source - Diseases Database)
A severe form of muscular dystrophy marked by generalized weakness and muscular wasting that affects the face and feet and hands and neck; difficult speech and difficulty with the hands that spreads to the arms and shoulders and legs and hips; the onset can be any time from birth to middle age and the progression is slow; inheritance is autosomal dominant
- (Source - WordNet 2.1)
Myotonic Dystrophy is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Myotonic Dystrophy, or a subtype of Myotonic Dystrophy,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Myotonic Dystrophy as a "rare disease".
Source - Orphanet
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