Giant axonal neuropathy

Giant axonal neuropathy
Giant axonal neuropathy
Classification and external resources
OMIM 256850
DiseasesDB 33515

Giant axonal neuropathy is a rare, autosomal recessive[1] neurological disorder that causes disorganization of neurofilaments. Neurofilaments form a structural framework that helps to define the shape and size of neurons and are essential for normal nerve function.

Contents

Diagnosis

Giant axonal neuropathy usually appears in infancy or early childhood, and is progressive. Early signs of the disorder often present in the peripheral nervous system, causing individuals with this disorder to have problems walking. Later, normal sensation, coordination, strength, and reflexes become affected. Hearing or vision problems may also occur. Abnormally kinky hair is characteristic of giant axonal neuropathy, appearing in almost all cases. As the disorder progresses, central nervous system becomes involved, which may cause a gradual decline in mental function, loss of control of body movement, and seizures.

Genetics

Giant axonal neuropathy has an autosomal recessive pattern of inheritance.

Giant axonal neuropathy results from mutations in the GAN gene, which codes for the protein gigaxonin. This alters the shape of the protein, changing how it interacts with other proteins when organizing the structure of the neuron.

Neurons affected by the altered protein accumulate excess neurofilaments in the axon, the long extension from the nerve cell that transmits its signal to other nerve cells and to muscles. These enlarged or 'giant' axons cannot transmit signals properly, and eventually deteriorate, resulting in the range of neurological anomalies associated with the disorder.

This disease is an autosomal recessive disorder, which means the defective gene is located on an autosome, and both parents must have one copy of the defective gene in order to have a child born with the disorder. The parents of a child with an autosomal recessive disorder are carriers, but are usually not affected by the disorder.

Sources

This article may incorporate some public domain text from The U.S. National Library of Medicine

External links

See also

References

  1. ^ Donaghy M, Brett EM, Ormerod IE, King RH, Thomas PK (July 1988). "Giant axonal neuropathy: observations on a further patient". Journal of neurology, neurosurgery, and psychiatry 51 (7): 991–4. doi:10.1136/jnnp.51.7.991. PMC 1033207. PMID 2849642. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1033207. 

Wikimedia Foundation. 2010.

Игры ⚽ Поможем сделать НИР

Look at other dictionaries:

  • giant axonal neuropathy — an autosomal recessive neuropathy of childhood due to mutation in the GAN gene (locus: 16q24.1), which encodes gigaxonin, a protein involved in the ubiquitin proteasome system targeting damaged proteins for destruction. There are central and… …   Medical dictionary

  • Neuropathy (disambiguation) — Neuropathy usually refers to peripheral neuropathy, which denotes damage to nerves of the peripheral nervous system. Neuropathy may also refer to: Cranial neuropathy, any condition affecting cranial nerves Auditory neuropathy, any condition… …   Wikipedia

  • Neuropathy — Any and all disease or malfunction of the nerves. * * * 1. A classical term for any disorder affecting any segment of the nervous system. 2. In contemporary usage, a disease involving the cranial nerves or the peripheral or autonomic nervous …   Medical dictionary

  • Optic neuropathy — Classification and external resources ICD 10 H46 The optic nerve contains axons of nerve cells that emerge from the retina, leave the eye at the optic disc, and go to the visual cortex where input from the eye is processed into vision. There are… …   Wikipedia

  • GAN (gene) — Giant axonal neuropathy (gigaxonin), also known as GAN, is a human gene. PBB Summary section title = summary text = This gene encodes a member of the cytoskeletal BTB/kelch (Broad Complex, Tramtrack and Bric a brac) repeat family. (Kelch repeats… …   Wikipedia

  • Charcot–Marie–Tooth disease — Charcot Marie Tooth disease Classification and external resources The foot of a person with Charcot Marie Tooth. The lack of muscle, a high arch, and claw toes are signs of the genetic disease. ICD 10 …   Wikipedia

  • Laminopathy — Normal nuclear lamina (a and b) and mutant nuclear lamina (c and d) from a patient with HGPS, visualized by immunofluorescence note the irregular and bumpy shape of the laminopathic nuclei[1] Laminopathies are a group of rare genetic disorders… …   Wikipedia

  • List of cutaneous conditions — This is an incomplete list, which may never be able to satisfy particular standards for completeness. You can help by expanding it with reliably sourced entries. See also: Cutaneous conditions, Category:Cutaneous conditions, and ICD 10… …   Wikipedia

  • Monilethrix — Classification and external resources ICD 10 Q84.1 (ILDS Q84.140) ICD 9 757.4 …   Wikipedia

  • Meesmann juvenile epithelial corneal dystrophy — Classification and external resources Multiple opaque spots in the corneal epithelium ICD …   Wikipedia

Share the article and excerpts

Direct link
Do a right-click on the link above
and select “Copy Link”