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Dictionary » Hypomyelinating polyneuropathy, congenital
 

Hypomyelinating polyneuropathy, congenital

Introduction: Hypomyelinating polyneuropathy, congenital

Description of Hypomyelinating polyneuropathy, congenital

Hypomyelinating polyneuropathy, congenital (medical condition): CMT is an inherited neurological disease characterized by the gradual...more »

See also:

Charcot-Marie-Tooth disease, Type 4E:
  »Introduction: Charcot-Marie-Tooth disease, Type 4E
  »Symptoms of Charcot-Marie-Tooth disease, Type 4E

Hypomyelinating polyneuropathy, congenital: Related Topics

These medical condition or symptom topics may be relevant to medical information for Hypomyelinating polyneuropathy, congenital:

Hypomyelinating polyneuropathy, congenital: Rare Disease

Ophanet

Ophanet, a consortium of European partners, currently defines a condition rare when if affects 1 person per 2,000. They list Hypomyelinating polyneuropathy, congenital as a "rare disease".

Source - Orphanet

Hypomyelinating polyneuropathy, congenital as a Disease

Hypomyelinating polyneuropathy, congenital: Another name for Charcot-Marie-Tooth disease, Type 4E (or close medical condition association).
  »Introduction: Charcot-Marie-Tooth disease, Type 4E
  »Symptoms of Charcot-Marie-Tooth disease, Type 4E

Hypomyelinating polyneuropathy, congenital: Related Diseases

Hypomyelinating polyneuropathy, congenital: Hypomyelinating polyneuropathy, congenital is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of Hypomyelinating polyneuropathy, congenital (Charcot-Marie-Tooth disease, Type 4E)

Some of the symptoms of Hypomyelinating polyneuropathy, congenital incude:

  • Infant hypotonia
  • Areflexia
  • Muscle weakness in extremities
  • Slow nerve conduction speed
  • Wasted muscles

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