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

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

Muscular dystrophy, limb-girdle, autosomal dominant, type 1G: An autosomal dominant form of limb-girdle muscular dystrophy where muscle weakness and atrophy is caused by mutations of chromosome 4p21. The muscle weakness and wasting progresses slowly and starts in the muscles closest to the trunk. More detailed information about the symptoms, causes, and treatments of Muscular dystrophy, limb-girdle, autosomal dominant, type 1G is available below.

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

  • Skeletal muscle weakness
  • Skeletal muscle atrophy
  • Progressive finger flexion
  • Progressive toe flexion
  • more symptoms...»

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

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

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

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

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Muscular dystrophy, limb-girdle, autosomal dominant, type 1G: Research Doctors & Specialists

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

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 1G as a "rare disease".
Source - Orphanet

Related Muscular dystrophy, limb-girdle, autosomal dominant, type 1G Info

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

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

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