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Dictionary » Myasthenia familial infantile
 

Myasthenia familial infantile

Introduction: Myasthenia familial infantile

Description of Myasthenia familial infantile

Myasthenia familial infantile (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

Myasthenia familial infantile: Related Topics

These medical condition or symptom topics may be relevant to medical information for Myasthenia familial infantile:

Myasthenia familial infantile: Rare Disease

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

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

Myasthenia familial infantile as a Disease

Myasthenia familial infantile: 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 Myasthenia familial infantile (Congenital myasthenic syndrome with episodic apnea)

Some of the symptoms of Myasthenia familial infantile incude:

See full list of 7 symptoms of Myasthenia familial infantile (Congenital myasthenic syndrome with episodic apnea)

Myasthenia familial infantile: Related Disease Topics

These medical disease topics may be related to Myasthenia familial infantile:

  • familial infantile myasthenia gravis
  • antimuscle antibodies

Terms associated with Myasthenia familial infantile:

Terms Similar to Myasthenia familial infantile:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

More Medical Dictionary Topics

  • 22q- syndrome
  • 22q11.2 deletion syndrome
  • 22SMC
  • 24 completed weeks of gestation
  • 24,25-Dihydroxyvitamin D 3
  • 24-dehydrocholesterol
  • 25 hydroxycholecalciferol
  • 25-26 completed weeks of gestation
  • 25-hydroxycholecalciferol (HCC)
  • 25-hydroxyergocalciferol
  • 25-Hydroxyvitamin D 2
  • 25-Hydroxyvitamin D-1-alpha-hydroxylase deficiency

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