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Types of Ataxia

Ataxia Telangiectasia
Ataxia Telangiectasia

Ataxia with Oculomotor Apraxia Type 1 and Type 2 (AOA1 and AOA2) have also been identified. What is Sporadic Ataxia? There is a large group of people who have symptoms of Ataxia that usually begin in adulthood and who have no known family history of the disease.

source: ataxia.org
Ataxia With Oculomotor Apraxia
Ataxia With Oculomotor Apraxia

Ataxia with oculomotor apraxia is a condition characterized by progressive problems with movement. The hallmark of this condition is difficulty coordinating movements (ataxia), which is often the first symptom. Most affected people also have oculomotor apraxia, which makes it difficult to move their eyes side-to-side.

Dominant Spastic Ataxias
Dominant Spastic Ataxias

Recessive Spastic Ataxias. Spastic ataxias are ataxias that have spasticity (muscle stiffness) in addition to ataxia. Some types of spastic ataxias are dominant and some are recessive. The recessive forms are described below. The acronym SPAX is used to name some of these ataxias (SPastic AtaXia).

Dominant Spinocerebellar Ataxias (SCA)
Dominant Spinocerebellar Ataxias (SCA)

Dominant Spinocerebellar Ataxias (SCA) There are many different types of Spinocerebellar Ataxia (SCA). These ataxias are all characterized by autosomal dominant inheritance. The primary feature of these disorders is ataxia (problems with balance, speech, and eye movements).

Episodic Ataxia
Episodic Ataxia

The word “ataxia” can also be used to describe a symptom of incoordination which can be associated with infections, injuries, other diseases, or degenerative changes in the central nervous system. This form of ataxia is different from the neurological disease.

source: ataxia.org
Friedreich's Ataxia
Friedreich's Ataxia

Friedreich ataxia (also called FA) is a rare inherited disease that causes progressive nervous system damage and movement problems. It usually begins in childhood and leads to impaired muscle coordination (ataxia) that worsens over time.

source: ninds.nih.gov
Recessive Spastic Ataxias
Recessive Spastic Ataxias

Autosomal recessive spastic ataxia of Charlevoix-Saguenay, more commonly known as ARSACS, is a condition affecting muscle movement. People with ARSACS typically have abnormal tensing of the muscles (spasticity), difficulty coordinating movements (ataxia), muscle wasting (amyotrophy), involuntary eye movements (nystagmus), and speech difficulties (dysarthria).

Wilson's Disease
Wilson's Disease

" Wilson's Disease - this is lack of copper- easy blood test for this one Thyroid- probably already checked but doesn't hurt to check T4 levels especially Potassium- believe it or not. Have dr. do a quick check of ...Hungitons Chorea Disease and Ataxia.

source: treato.com