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Dictionary » EMG syndrome
 

EMG syndrome

Introduction: EMG syndrome

Description of EMG syndrome

EMG syndrome (medical condition): A rare genetic disorder characterized by macroglossia...more »

See also:

Beckwith-Wiedemann Syndrome:
  »Introduction: Beckwith-Wiedemann Syndrome
  »Symptoms of Beckwith-Wiedemann Syndrome

EMG syndrome: An inherited disorder marked by gigantism, exomphalos and macroglossia. Also called Beckwith-Wiedemann syndrome and exophthalmos-macroglossia-gigantism syndrome.

EMG syndrome: Related Topics

These medical condition or symptom topics may be relevant to medical information for EMG syndrome:

EMG syndrome: Rare Disease

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

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

EMG syndrome as a Disease

EMG syndrome: Another name for Beckwith-Wiedemann Syndrome (or close medical condition association).
  »Introduction: Beckwith-Wiedemann Syndrome
  »Symptoms of Beckwith-Wiedemann Syndrome

EMG syndrome: Related Diseases

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

Symptoms of EMG syndrome (Beckwith-Wiedemann Syndrome)

Some of the symptoms of EMG syndrome incude:

  • Mental deficiency
  • Large body size
  • Large muscle mass
  • Thick subcutaneous tissue
  • Accelerated osseous maturation

EMG syndrome: Related Disease Topics

These medical disease topics may be related to EMG syndrome:

Terms associated with EMG syndrome:

Terms Similar to EMG syndrome:

Source - NIH

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