CMS1D

Introduction: CMS1D

Description of CMS1D

CMS1D (medical condition): A genetic, nonprogressive neuromuscular disorder causing muscle weakness. The severity of symptoms is variable and stress and illness can exacerbate symptoms.

See also:

Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency:
  »Introduction: Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency
  »Symptoms of Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency
  »Treatments for Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency

CMS1D as a Disease

CMS1D: Another name for Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency (or close medical condition association).
  »Introduction: Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency
  »Symptoms of Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency
  »Treatments for Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency

Symptoms of CMS1D (Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency)

Some of the symptoms of CMS1D incude:

• Long face
• Protruding jaw
• Facial muscle weakness
• Droopy eyelids
• Weak eye muscles

See full list of 25 symptoms of CMS1D (Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency)

Treatments for CMS1D (Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency)

Treatments for CMS1D (Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency) include:

• Anticholinesterase therapy can improve symptoms in most cases

Read more about treatments for CMS1D

Treatment of CMS1D: For more treatment information about CMS1D, see treatment of Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency (CMS1D)

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Medical dictionaries:

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