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Muscular dystrophy congenital, merosin negative

Muscular dystrophy congenital, merosin negative: Introduction

Muscular dystrophy congenital, merosin negative: A rare group of diseases characterized mainly by reduced muscle tone and muscle weakness in the arms, legs and trunk. Symptoms start at birth or soon after. More detailed information about the symptoms, causes, and treatments of Muscular dystrophy congenital, merosin negative is available below.

Symptoms of Muscular dystrophy congenital, merosin negative

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Muscular dystrophy congenital, merosin negative: Related Patient Stories

Causes of Muscular dystrophy congenital, merosin negative

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Muscular dystrophy congenital, merosin negative: Undiagnosed Conditions

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Misdiagnosis and Muscular dystrophy congenital, merosin negative

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Muscular dystrophy congenital, merosin negative: Research Doctors & Specialists

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Hospitals & Clinics: Muscular dystrophy congenital, merosin negative

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Definitions of Muscular dystrophy congenital, merosin negative:

Muscular dystrophy congenital, merosin negative is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Muscular dystrophy congenital, merosin negative, or a subtype of Muscular dystrophy congenital, merosin negative, 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 Muscular dystrophy congenital, merosin negative as a "rare disease".
Source - Orphanet

 

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