Limb-girdle muscular dystrophy type 2D
Limb-girdle muscular dystrophy type 2D: Introduction
Limb-girdle muscular dystrophy type 2D: An autosomal recessive form of limb-girdle muscular dystrophy where muscle weakness and atrophy is caused by mutations of the alpha-sarcoglycan gene. The severity of the condition is greatly variable from wheelchair confinement at the age of 9 years to asymptomatic adults. Most tend to live to their third decade.
More detailed information about the symptoms,
causes, and treatments of Limb-girdle muscular dystrophy type 2D is available below.
Symptoms of Limb-girdle muscular dystrophy type 2D
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symptoms of Limb-girdle muscular dystrophy type 2D
Wrongly Diagnosed with Limb-girdle muscular dystrophy type 2D?
Limb-girdle muscular dystrophy type 2D: Deaths
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Limb-girdle muscular dystrophy type 2D: Complications
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Causes of Limb-girdle muscular dystrophy type 2D
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Disease Topics Related To Limb-girdle muscular dystrophy type 2D
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Less Common Symptoms of Limb-girdle muscular dystrophy type 2D
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Misdiagnosis and Limb-girdle muscular dystrophy type 2D
Leg cramps at night a classic sign: The symptom of having leg muscle cramps,
particularly at night, is a classic sign of undiagnosed diabetes.
However, there are also various other causes.
See ...read more »
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Limb-girdle muscular dystrophy type 2D: Research Doctors & Specialists
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- Arthritis & Joint Health Specialists (Rheumatology):
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Limb-girdle muscular dystrophy type 2D: Animations
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Prognosis for Limb-girdle muscular dystrophy type 2D
Prognosis for Limb-girdle muscular dystrophy type 2D:
severe cases are confined to wheelchair by 13 years whereas as milder cases are capable of walking even after 16 years of age
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Limb-girdle muscular dystrophy type 2D: Broader Related Topics
Types of Limb-girdle muscular dystrophy type 2D
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