Other hereditary ataxias digital illustration

Other hereditary ataxias Save


ICD-10 code: G11.8

Disease category: G11: Hereditary ataxia

Understanding Other Hereditary Ataxias

Ataxia refers to a group of neurological disorders that affect coordination, balance, and movement control. While many people are familiar with the most common form of ataxia, known as spinocerebellar ataxia (SCA), there are several other types of hereditary ataxias that also deserve attention. In this article, we will explore some of these lesser-known forms of ataxia and their key features.

  1. Friedreich's Ataxia (FRDA)

    FRDA is the most prevalent form of hereditary ataxia. It typically manifests in childhood and gradually progresses over time. Individuals with FRDA experience a variety of symptoms, including muscle weakness, impaired coordination, and loss of sensation in the arms and legs. Cardiac abnormalities and scoliosis are also common in FRDA patients.

  2. Ataxia Telangiectasia (AT)

    AT is a rare genetic disorder characterized by progressive neurological problems. Children with AT often present with poor coordination, balance issues, and a weakened immune system. They may also develop dilated blood vessels (telangiectasias), which appear as small red spider-like clusters on the skin or eyes. AT patients have a higher risk of developing cancer and other respiratory infections.

  3. Episodic Ataxia (EA)

    EA is a rare form of hereditary ataxia that causes recurrent episodes of unsteadiness and uncoordinated movement. These episodes can last anywhere from minutes to hours and may be triggered by stress, fatigue, or certain medications. EA can be classified into several subtypes, with each one having unique characteristics and triggers.

  4. Multiple System Atrophy (MSA)

    MSA is a progressive neurodegenerative disorder that affects multiple systems within the body. It is often characterized by symptoms such as ataxia, autonomic dysfunction, and parkinsonism. MSA can be further categorized into two main types: MSA with predominant cerebellar ataxia (MSA-C) and MSA with predominant parkinsonism (MSA-P).

While these are just a few examples of other hereditary ataxias, it's important to remember that each type has its own unique features and diagnostic criteria. If you suspect you or someone you know may have a hereditary ataxia, it is crucial to consult with a medical professional for an accurate diagnosis and appropriate management strategies.

Please note

Treatment of Other hereditary ataxias:

Treatment Options for Other Hereditary Ataxias

Hereditary ataxias are a group of genetic disorders that affect coordination and balance. While there is no cure for these conditions, several treatment options can help manage the symptoms and improve the quality of life for individuals with other hereditary ataxias.

  1. Physical therapy: Physical therapy ...

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