MDC1A

Introduction: MDC1A

Description of MDC1A

MDC1A (medical condition): A rare group of diseases characterized mainly by reduced...more »

See also:

Muscular dystrophy congenital, merosin negative:
  »Introduction: Muscular dystrophy congenital, merosin negative
  »Symptoms of Muscular dystrophy congenital, merosin negative

MDC1A: Rare Disease

Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

MDC1A is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that MDC1A, or a subtype of MDC1A, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

MDC1A as a Disease

MDC1A: Another name for Muscular dystrophy congenital, merosin negative (or close medical condition association).
  »Introduction: Muscular dystrophy congenital, merosin negative
  »Symptoms of Muscular dystrophy congenital, merosin negative

MDC1A: Related Diseases

MDC1A: MDC1A is listed as a type of (or associated with) the following medical conditions in our database:

• Neuromuscular conditions
• Muscle conditions
• Musculoskeletal conditions
• Limb conditions
• Genetic conditions

Symptoms of MDC1A (Muscular dystrophy congenital, merosin negative)

Some of the symptoms of MDC1A incude:

• Reduced muscle tone
• Muscle weakness
• Muscular retraction
• Delayed motor development
• Brain abnormalities on MRI

See full list of 6 symptoms of MDC1A (Muscular dystrophy congenital, merosin negative)

Terms associated with MDC1A:

Terms Similar to MDC1A:

• Merosin-deficient congenital muscular dystrophy
• Merosin-negative congenital muscular dystrophy
• Muscular dystrophy, congenital, merosin-deficient 1A
• Muscular dystrophy congenital, merosin negative

Source - NIH

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