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What is Neuropathy, distal hereditary motor, type VIIA?

What is Neuropathy, distal hereditary motor, type VIIA?

  • Neuropathy, distal hereditary motor, type VIIA: An inherited neuromuscular disease that causes progressive muscle wasting and weakness in the limbs and vocal cord paralysis. There is no sensory impairment.

Neuropathy, distal hereditary motor, type VIIA: Introduction

Types of Neuropathy, distal hereditary motor, type VIIA:

Broader types of Neuropathy, distal hereditary motor, type VIIA:

How serious is Neuropathy, distal hereditary motor, type VIIA?

Prognosis of Neuropathy, distal hereditary motor, type VIIA: The condition is slowly progressive with muscle wasting affecting the hands first.

What causes Neuropathy, distal hereditary motor, type VIIA?

Causes of Neuropathy, distal hereditary motor, type VIIA: see causes of Neuropathy, distal hereditary motor, type VIIA

What are the symptoms of Neuropathy, distal hereditary motor, type VIIA?

Symptoms of Neuropathy, distal hereditary motor, type VIIA: see symptoms of Neuropathy, distal hereditary motor, type VIIA

Onset of Neuropathy, distal hereditary motor, type VIIA: usually during the second decade

Neuropathy, distal hereditary motor, type VIIA: Testing

Diagnostic testing: see tests for Neuropathy, distal hereditary motor, type VIIA.

Misdiagnosis: see misdiagnosis and Neuropathy, distal hereditary motor, type VIIA.

How is it treated?

Doctors and Medical Specialists for Neuropathy, distal hereditary motor, type VIIA: Medical Geneticist, Neurologist ; see also doctors and medical specialists for Neuropathy, distal hereditary motor, type VIIA.
Treatments for Neuropathy, distal hereditary motor, type VIIA: see treatments for Neuropathy, distal hereditary motor, type VIIA

Name and Aliases of Neuropathy, distal hereditary motor, type VIIA

Main name of condition: Neuropathy, distal hereditary motor, type VIIA

Other names or spellings for Neuropathy, distal hereditary motor, type VIIA:

spinal muscular atrophy, distal, with vocal cord paralysis, HMN7A, Harper-Young myopathy

 

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