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Neuropathy, hereditary motor and sensory, Okinawa type

Neuropathy, hereditary motor and sensory, Okinawa type: Introduction

Neuropathy, hereditary motor and sensory, Okinawa type: A dominantly inherited, slow-progressing motor and sensory nerve disease which primarily involves the proximal muscles (i.e. the muscles closest to the trunk of the body). More detailed information about the symptoms, causes, and treatments of Neuropathy, hereditary motor and sensory, Okinawa type is available below.

Symptoms of Neuropathy, hereditary motor and sensory, Okinawa type

Home Diagnostic Testing

Home medical testing related to Neuropathy, hereditary motor and sensory, Okinawa type:

Wrongly Diagnosed with Neuropathy, hereditary motor and sensory, Okinawa type?

Causes of Neuropathy, hereditary motor and sensory, Okinawa type

Read more about causes of Neuropathy, hereditary motor and sensory, Okinawa type.

Neuropathy, hereditary motor and sensory, Okinawa type: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

In-Depth Reports: Diagnosis and Misdiagnosis

Diabetes diagnosis and misdiagnosis (In-Depth Report): Detailed report on diabetes misdiagnoses, rare curable types, and less common diagnostic issues....read full report »

Misdiagnosis and Neuropathy, hereditary motor and sensory, Okinawa type

Metabolic syndrome often undiagnosed: Metabolic syndrome, also known as Syndrome X, is an often overlooked medical condition that causes a cluster of chronic symptoms. There are often four symptoms and...read more »

Heart attacks can be undiagnosed: Although the most severe symptoms of heart attack are hard to miss, there are varying degrees of severity. It is altogether too common for people to die...read more »

Heart attacks can be overdiagnosed: Although many people die from heart attacks, there are also many cases where people fear that they have a heart attack, but...read more »

Cluster of diseases with difficult diagnosis issues: There is a well-known list of medical conditions that are all somewhat difficult to diagnose, and all can present in a variety of...read more »

Poorly healing leg rashes a classic sign of chronic disease: Recurring leg rashes, or poorly healing leg rashes, are a classic sign of undiagnosed diabetes, particularly of ...read more »

Leg cramps at night a classic sign: The symptom of having leg muscle cramps, particularly at night, is a classic sign of undiagnosed diabetes. However,...read more »

Obesity-related conditions undiagnosed in children: A variety of conditions are associated with obesity (see obesity), but these tend to be undiagnosed more often in child patients than in adults. Some of the...read more »

Vitamin B12 deficiency under-diagnosed: The condition of Vitamin B12 deficiency is a possible misdiagnosis of various conditions, such as multiple sclerosis (see symptoms of multiple...read more »

Neuropathy, hereditary motor and sensory, Okinawa type: Research Doctors & Specialists

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Hospitals & Clinics: Neuropathy, hereditary motor and sensory, Okinawa type

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Choosing the Best Hospital: More general information, not necessarily in relation to Neuropathy, hereditary motor and sensory, Okinawa type, on hospital performance and surgical care quality:

Neuropathy, hereditary motor and sensory, Okinawa type: Rare Types

Rare types of diseases and disorders in related medical categories:

Neuropathy, hereditary motor and sensory, Okinawa type: Animations

Prognosis for Neuropathy, hereditary motor and sensory, Okinawa type

Prognosis for Neuropathy, hereditary motor and sensory, Okinawa type: The disease progresses slowly - patients may be bedridden within two decades of onset

Neuropathy, hereditary motor and sensory, Okinawa type: Broader Related Topics

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Related Neuropathy, hereditary motor and sensory, Okinawa type Info

More information about Neuropathy, hereditary motor and sensory, Okinawa type

  1. Neuropathy, hereditary motor and sensory, Okinawa type: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
  7. Types
  8. Prognosis
 

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