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Muscular dystrophy, limb-girdle, autosomal dominant, type 1F

Muscular dystrophy, limb-girdle, autosomal dominant, type 1F: Introduction

Muscular dystrophy, limb-girdle, autosomal dominant, type 1F: An autosomal dominant form of limb-girdle muscular dystrophy where muscle weakness and atrophy is caused by mutations of chromosome 7q31.1. The muscle weakness starts in the muscles close to the trunk and spreads to the ends of the limbs. Early onset may result in wheelchair dependence by the 4th decade. The rate of progression is variable. More detailed information about the symptoms, causes, and treatments of Muscular dystrophy, limb-girdle, autosomal dominant, type 1F is available below.

Symptoms of Muscular dystrophy, limb-girdle, autosomal dominant, type 1F

Wrongly Diagnosed with Muscular dystrophy, limb-girdle, autosomal dominant, type 1F?

Causes of Muscular dystrophy, limb-girdle, autosomal dominant, type 1F

Read more about causes of Muscular dystrophy, limb-girdle, autosomal dominant, type 1F.

Misdiagnosis and Muscular dystrophy, limb-girdle, autosomal dominant, type 1F

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Definitions of Muscular dystrophy, limb-girdle, autosomal dominant, type 1F:

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Muscular dystrophy, limb-girdle, autosomal dominant, type 1F as a "rare disease".
Source - Orphanet

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More information about Muscular dystrophy, limb-girdle, autosomal dominant, type 1F

  1. Muscular dystrophy, limb-girdle, autosomal dominant, type 1F: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
 

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