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Friedreich's ataxia

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Friedreich's ataxia
ICD-10 G111
ICD-9 334.0
OMIM 229300
DiseasesDB 4980
MedlinePlus [1]
eMedicine neuro/139
MeSH {{{MeshNumber}}}

Friedreich's ataxia is an inherited disease that causes progressive damage to the nervous system resulting in symptoms ranging from gait disturbance and speech problems to heart disease.

Generally, ataxia is a symptom of coordination problems such as clumsy or awkward movements and unsteadiness and occurs in many different diseases and conditions. The ataxia of Friedreich's ataxia results from the degeneration of nerve tissue in the spinal cord, in particular sensory neurons essential (through connections with the cerebellum) for directing muscle movement of the arms and legs. The spinal cord becomes thinner and nerve cells lose some of their myelin sheath (the insular covering on some nerve cells that helps conduct nerve impulses).

EponymEdit

The condition is named after the German physician Nicholaus Friedreich, who first described it in the 1860s.[1]

PrevalenceEdit

Friedreich's ataxia is the most prevalent inherited ataxia, affecting about 1 in 50,000 people in the United States. Males and females are affected equally. The estimated carrier prevalence is 1:110.

A 1984 Canadian study was able to trace 40 cases of classical Friedreich's disease from 14 French-Canadian kindreds previously thought to be unrelated to one common ancestral couple arriving in New France in 1634: Jean Guyon and Mathurine Robin.[2]

About 20 percent of people with Friedreich's ataxia develop carbohydrate intolerance and 10 percent develop diabetes mellitus.

GeneticsEdit

Autorecessive

Friedreich's ataxia has an autosomal recessive pattern of inheritance.

Friedreich's ataxia is an autosomal recessive congenital ataxia and is caused by a mutation in gene FXN (formerly known as X25[3]) that codes for frataxin, located on chromosome 9. This protein is essential for proper functioning of mitochondria (it has been shown to be connected with the removal of iron from the cytoplasm surrounding the mitochondria, and in the absence of frataxin, the iron builds up and causes free radical damage). Nerve and muscle cells appear to be particularly sensitive to the deleterious effects of this type of mitochondrial dysfunction.

The classic form of Friedreich's ataxia has been mapped to a gene on 9q13-q21 that affects production of the protein frataxin. In most cases, the mutant gene contains expanded GAA triplet repeats in the first intron; in a few pedigrees, point mutations have been detected. Because the defect is located on an intron (which is removed from the mRNA transcript between transcription and translation), this mutation does not result in the production of abnormal frataxin proteins. Instead, the mutation causes gene silencing (i.e., the mutation decreases the transcription of the gene) through induction of a heterochromatin structure in a manner similar to position-effect variegation.

Relationship to muscular dystrophyEdit

Friedreich's ataxia and the muscular dystrophy family of neuromuscular diseases, though often compared, are different diseases. Muscular dystrophies are the result of muscle tissue degeneration and atrophy, whereas Friedreich's ataxia is the result of nerve degeneration caused by a trinucleotide repeat expansion mutation. Research on both disorders is supported by funding from the Muscular Dystrophy Association.

Symptoms Edit

Symptoms typically begin sometime between the ages of 5 to 15 years, but in Late Onset FA may occur in the 20s or 30s. Symptoms include any combination, but not necessarily all, of the following:

It presents before 25 years of age with progressive staggering or stumbling gait and frequent falling. Lower extremities are more severely involved.

These symptoms are slow and progressive. Long-term observation shows that many patients reach a plateau in symptoms in the patient's early adulthood.

SignsEdit

20% of cases are found in association with diabetes mellitus type 1 or 2 or pancreatic β cell dysfunction.

PathogenesisEdit

The primary site of pathology is spinal cord and peripheral nerves. Sclerosis and degeneration of dorsal root ganglion, spinocerebellar tracts, lateral corticospinal tracts, and posterior columns[4]. In peripheral nerves there is a loss of large myelinated fibres.

Treatment Edit

Currently, there is a treatment approved in Canada called Catena (idebenone) . This prescription medicine is also under regulatory review in the European Union and Switzerland. In both the United States and in Europe there are two Phase III clinical trials on-going with idebenone .[5]

A person suffering from Friedrich's Ataxia may require some surgical interventions (mainly for the spine and heart). Often a metal rod is inserted in the spine to help prevent or slow the progression of scoliosis. As progression of ataxia occurs, assistive devices such as a cane, walker, or wheelchair are required for mobility and independence. Other assistive technology, such as a standing frame, can help reduce the secondary complications of prolonged use of a wheelchair.

In many cases, patients experience significant heart conditions as well. These conditions, fortunately, are much more treatable, and are often countered with ACE inhibitors such as enalapril or lisinopril and other heart medications such as digoxin.

See also Edit


External links Edit

ReferencesEdit

  1. Who Named It synd/1406
  2. Barbeau A, Sadibelouiz M, Roy M, Lemieux B, Bouchard JP, Geoffroy G (1984). Origin of Friedreich's disease in Quebec. The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 11 (4 Suppl): 506–9.
  3. http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=606829
  4. Delatycki M, Williamson R, Forrest S (2000). Friedreich ataxia: an overview. J Med Genet 37 (1): 1–8 As.
  5. http://www.clinicaltrials.gov/ct2/results?term=idebenone+friedreich%27s+idebenone
  6. Delatycki M, Williamson R, Forrest S (2000). Friedreich ataxia: an overview. J Med Genet 37 (1): 1–8 As.
  1. REDIRECT Template:CNS diseases of the nervous system

Template:Mitochondrial diseases Template:Trinucleotide repeat disorders

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