CMS-EA

Introduction: CMS-EA

Description of CMS-EA

CMS-EA (medical condition): A disorder characterized by muscular weakness.

See also:

Congenital myasthenic syndrome with episodic apnea:
  »Introduction: Congenital myasthenic syndrome with episodic apnea
  »Symptoms of Congenital myasthenic syndrome with episodic apnea

CMS-EA: Rare Disease

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

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

CMS-EA as a Disease

CMS-EA: Another name for Congenital myasthenic syndrome with episodic apnea (or close medical condition association).
  »Introduction: Congenital myasthenic syndrome with episodic apnea
  »Symptoms of Congenital myasthenic syndrome with episodic apnea

Symptoms of CMS-EA (Congenital myasthenic syndrome with episodic apnea)

Some of the symptoms of CMS-EA incude:

• Fluctuating ptosis
• Poor infant sucking
• Weak infant cry
• Infant feeding difficulties
• Secondary respiratory infections

See full list of 7 symptoms of CMS-EA (Congenital myasthenic syndrome with episodic apnea)

CMS-EA: Related Disease Topics

These medical disease topics may be related to CMS-EA:

• familial infantile myasthenia gravis
• antimuscle antibodies

Terms associated with CMS-EA:

Terms Similar to CMS-EA:

• CMS1A
• Congenital myasthenic syndrome type 1a
• FIM
• FIMG2 (formerly)
• Myasthenia familial infantile
• Myasthenia gravis familial infantile 2 (formerly)
• Myasthenic syndrome congenital associated with episodic apnea
• Myasthenic syndrome, presynaptic, congenital, associated with episodic apnea
• Congenital myasthenic syndrome with episodic apnea

Source - NIH

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Medical dictionaries:

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