Neuroacanthocytosis
Neuroacanthocytosis: Introduction
Neuroacanthocytosis: An autosomal recessive syndrome characterized by tics, chorea, and personality changes.
More detailed information about the symptoms,
causes, and treatments of Neuroacanthocytosis is available below.
Symptoms of Neuroacanthocytosis
See full list of 22
symptoms of Neuroacanthocytosis
Home Diagnostic Testing
Home medical testing related to Neuroacanthocytosis:
- Nerve Neuropathy: Related Home Testing:
- more...»
Wrongly Diagnosed with Neuroacanthocytosis?
Neuroacanthocytosis: Related Patient Stories
Neuroacanthocytosis: Complications
Read more about complications of Neuroacanthocytosis.
Causes of Neuroacanthocytosis
Read more about causes of Neuroacanthocytosis.
Disease Topics Related To Neuroacanthocytosis
Research the causes of these diseases that are similar to, or related to, Neuroacanthocytosis:
Neuroacanthocytosis: Undiagnosed Conditions
Commonly undiagnosed diseases in related medical categories:
Misdiagnosis and Neuroacanthocytosis
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 »
Read more about Misdiagnosis and Neuroacanthocytosis
Neuroacanthocytosis: Research Doctors & Specialists
Research related physicians and medical specialists:
Other doctor, physician and specialist research services:
Statistics for Neuroacanthocytosis
Neuroacanthocytosis: Broader Related Topics
Types of Neuroacanthocytosis
User Interactive Forums
Read about other experiences, ask a question about Neuroacanthocytosis, or answer someone else's question, on our message boards:
Definitions of Neuroacanthocytosis:
Neuroacanthocytosis is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Neuroacanthocytosis, or a subtype of Neuroacanthocytosis,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Neuroacanthocytosis as a "rare disease".
Source - Orphanet
Contents for Neuroacanthocytosis: