CMS1A

Introduction: CMS1A

Description of CMS1A

CMS1A (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

CMS1A: Rare Disease

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

CMS1A is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that CMS1A, or a subtype of CMS1A, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

CMS1A as a Disease

CMS1A: 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 CMS1A (Congenital myasthenic syndrome with episodic apnea)

Some of the symptoms of CMS1A incude:

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

See full list of 7 symptoms of CMS1A (Congenital myasthenic syndrome with episodic apnea)

CMS1A: Related Disease Topics

These medical disease topics may be related to CMS1A:

• familial infantile myasthenia gravis
• antimuscle antibodies

Terms associated with CMS1A:

Terms Similar to 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
• CMS-EA

Source - NIH

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