Giant axonal neuropathy

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Overview[edit | edit source]

Giant Axonal Neuropathy (GAN) is a rare genetic disorder that affects the nervous system. It is characterized by the abnormal growth of axons, which are the long, threadlike extensions of neurons that transmit nerve impulses. This condition is inherited in an autosomal recessive pattern, meaning that both copies of the gene in each cell have mutations.

Pathophysiology[edit | edit source]

GAN is caused by mutations in the GAN gene, which provides instructions for making a protein called gigaxonin. This protein is involved in the breakdown of intermediate filaments, which are part of the cell's cytoskeleton. In individuals with GAN, the abnormal gigaxonin leads to the accumulation of intermediate filaments in the axons, causing them to swell and become dysfunctional.

Clinical Features[edit | edit source]

The symptoms of Giant Axonal Neuropathy typically begin in early childhood. Affected individuals often experience:

Diagnosis[edit | edit source]

Diagnosis of GAN is based on clinical evaluation, family history, and genetic testing. Nerve biopsy may reveal the characteristic giant axons filled with disorganized neurofilaments. Genetic testing can confirm mutations in the GAN gene.

Management[edit | edit source]

There is currently no cure for Giant Axonal Neuropathy. Management focuses on symptomatic treatment and supportive care, including:

Prognosis[edit | edit source]

The progression of GAN varies among individuals, but it is generally a progressive disorder. Most affected individuals experience a decline in motor and sensory functions over time, leading to significant disability.

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Contributors: Prab R. Tumpati, MD