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What is Arthrogryposis, congenital -- myopathic seizures?

What is Arthrogryposis, congenital -- myopathic seizures?

  • Arthrogryposis, congenital -- myopathic seizures: A rare syndrome characterized by mental retardation and muscle problems.

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Arthrogryposis, congenital -- myopathic seizures as a "rare disease".
Source - Orphanet

Arthrogryposis, congenital -- myopathic seizures: Introduction

What are the symptoms of Arthrogryposis, congenital -- myopathic seizures?

Symptoms of Arthrogryposis, congenital -- myopathic seizures: see symptoms of Arthrogryposis, congenital -- myopathic seizures

Arthrogryposis, congenital -- myopathic seizures: Testing

Diagnostic testing: see tests for Arthrogryposis, congenital -- myopathic seizures.

Misdiagnosis: see misdiagnosis and Arthrogryposis, congenital -- myopathic seizures.

How is it treated?

Doctors and Medical Specialists for Arthrogryposis, congenital -- myopathic seizures: Pediatrician ; see also doctors and medical specialists for Arthrogryposis, congenital -- myopathic seizures.
Treatments for Arthrogryposis, congenital -- myopathic seizures: see treatments for Arthrogryposis, congenital -- myopathic seizures

Name and Aliases of Arthrogryposis, congenital -- myopathic seizures

Main name of condition: Arthrogryposis, congenital -- myopathic seizures

Other names or spellings for Arthrogryposis, congenital -- myopathic seizures:

Kalyanaraman syndrome

 

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