Anti-IgLON5 disease

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Anti-IgLON5 disease
Synonyms
Pronounce N/A
Specialty Neurology
Symptoms Sleep disorder, movement disorder, cognitive dysfunction, bulbar dysfunction
Complications N/A
Onset Typically in adulthood
Duration Chronic
Types N/A
Causes Autoimmune disease
Risks
Diagnosis Clinical diagnosis, antibody testing
Differential diagnosis Neurodegenerative disease, other autoimmune encephalitis
Prevention N/A
Treatment Immunotherapy, symptomatic treatment
Medication N/A
Prognosis Variable, often progressive
Frequency Rare
Deaths N/A


A rare neurological disorder associated with sleep disturbances and neurodegeneration


Anti-IgLON5 disease is a rare neurological disorder characterized by a combination of sleep disturbances, movement disorders, and neurodegeneration. It is associated with the presence of antibodies against the IgLON5 protein, which is involved in cell adhesion in the nervous system.

Pathophysiology

Anti-IgLON5 disease is an autoimmune disorder where the body's immune system mistakenly attacks the IgLON5 protein. This protein is part of the IgLON family of cell adhesion molecules, which play a crucial role in the development and maintenance of the central nervous system. The presence of anti-IgLON5 antibodies leads to neuroinflammation and neurodegeneration, particularly affecting the brainstem and hypothalamus.

Clinical Features

The clinical presentation of anti-IgLON5 disease is diverse, but it primarily affects sleep and movement. Common symptoms include:

Diagnosis

Diagnosis of anti-IgLON5 disease involves a combination of clinical evaluation, neuroimaging, and laboratory tests. The presence of anti-IgLON5 antibodies in the cerebrospinal fluid or serum is a key diagnostic marker. MRI scans may show atrophy in specific brain regions, and polysomnography can be used to assess sleep disturbances.

Treatment

There is currently no cure for anti-IgLON5 disease, and treatment focuses on managing symptoms. Options may include:

Prognosis

The prognosis of anti-IgLON5 disease varies. Some patients experience a slow progression of symptoms, while others may have a more rapid decline. The disease can lead to significant disability and may be life-threatening due to complications such as severe sleep apnea.

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Contributors: Prab R. Tumpati, MD