Autosomal recessive cerebellar ataxia

Autosomal recessive cerebellar ataxia type 1 (ARCA1) is a condition characterized by progressive problems with movement. Signs and symptoms of the disorder first appear in early to mid-adulthood. People with this condition initially experience impaired speech (dysarthria), problems with coordination and balance (ataxia), or both. They may also have difficulty with movements that involve judging distance or scale (dysmetria). Other features of ARCA1 include abnormal eye movements (nystagmus) and problems following the movements of objects with their eyes. The movement problems are slowly progressive, often resulting in the need for a cane, walker, or wheelchair.[1]

ARCA1

ARCA1 is caused by the mutated SYNE1 gene that is vital for the synthesis of Syne-1 protein in the Purkinje cells of the cerebellum. Deformed Syne-1 protein disrupts normal Purkinje cell functions and impairs its signalling with cerebellar neurons. To date it is still vague to how the impaired syne-1 proteins leads to the loss of cells in the cerebellum that contribute to ARCA1. Autosomal Recessive Ataxia Type 1 [2]

Different types of Ataxia:

Characteristics

Most cases of autosomal recessive cerebellar ataxia are early onset, usually around the age of 20. People with this type of ataxia share many characteristic symptoms including:

Autosomal recessive ataxias are generally associated with a loss of proprioreception and vibration sense. Arreflexia is more common in autosomal recessive ataxia than autosomal dominant ataxias. Also, they tend to have more involvement outside of the nervous system.[3] Mutations in subunit of the mitochondrial DNA polymerase (POLG) have been found to be a potential cause of autosomal recessive cerebellar ataxia.[4]

Life with Ataxia

In most cases, between the age of 2 and 4 oculomotor signals are present. Between the age of 2 and 8, Teleangiectasias appears. Usually by the age of 10 the child needs a wheel chair. Individuals with autosomal recessive cerebellum ataxia usually survive till their 20s; in some cases individuals have survived till their 40s or 50s.

Oculomotor ataxia accompanies gait ataxia which causes dysarthria, muscle weakeness, loss of joint position sense and limb dysmetria. In some cases, patients have shown mental retardation and loss of myelinated axons.

Ataxia with Telaniectasia is a rare form ataxia that causes chromosomal instability, sensitivity to ionizing radiation, disrupted stress-activated signal transduction pathways and radioresistant DNA synthesis.

[5]

Diagnosis

Clinical diagnosis is conducted on individuals with age onset between late teens and late forties who show the initial characteristics for the recessive autosomal cerebellar ataxia. The following tests are performed:

Prenatal diagnosis and preimplantation genetic diagnosis (PGD) can be performed to identify the mothers carrying the recessive genes for cerebellar ataxia.

Treatments

[6]

Unsolved Problems

The genes that underlie majority of the symptoms for the different types of Ataxia are still unknown. A productive cure is still unavailable to prevent the brain degeneration associated with ataxia.

[6]

Notes

  1. ↑ "Autosomal recessive cerebellar ataxia type 1". Retrieved November 26, 2012.
  2. ↑ "Autosomal recessive cerebellar Ataxia." Web. http://ghr.nlm.nih.gov/condition/autosomal-recessive-cerebellar-ataxia-type-1
  3. ↑ Fogel, Clinical Features and Molecular Genetics of ARCA
  4. ↑ Hakonen, Mitochondrial DNA Mutation
  5. ↑ "Autosomal Recessive Cerebellar Ataxias." Fracis, Palau" BioMed Central. Orphanet Journal of Rare Diseases
  6. 1 2 "Autosomal Recessive Cerebellar Ataxias." Fracis, Palau

References

This article incorporates text from the United States National Library of Medicine, which is in the public domain.

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