Neuroacanthocytosis syndromes may be classified into 2 main categories:
- Core syndromes (ie, McLeod syndrome, chorea-acanthocytosis syndrome)
- Diseases of abnormal lipoprotein metabolism (ie, abetalipoproteinemia)
Chorea-acanthocytosis syndrome is an autosomal recessive disorder. It presents in the third decade of life and has a slowly progressive course over 15-30 years. Psychiatric symptoms and subtle cognitive changes often occur years prior to abnormal movements. Abnormal movements include chorea, orofaciolingual dystonia (leading to feeding difficulties), limb dystonia, and sometimes parkinsonism. Axonal neuropathy and myopathy may occur but are often mild. Cardiac disease typically does not occur. However, sudden unexplained deaths have been reported.
Abetalipoproteinemia is an autosomal recessive disorder. It typically presents in infancy and, if untreated, symptoms progress over time. With appropriate treatment, patients can live into adulthood with minimal symptoms. Initial symptoms include failure to thrive, diarrhea, and vomiting. Acanthocytes are often present and lead to a hemolytic anemia and hyperbilirubinemia. Malabsorption of fat-soluble vitamins can lead to increased bleeding. Untreated children eventually develop pigmentation of the retina (which may lead to vision loss) and a neuropathy (which may lead to a sensory ataxia).
These disorders are rare but may also be underdiagnosed. Each disorder is estimated to affect approximately 1-5 per million people worldwide.
Q99.8 – Other specified chromosome abnormalities
66881004 – Choreoacanthocytosis
724172004 – McLeod neuroacanthocytosis syndrome
724770001 – Ataxia co-occurrent and due to abetalipoproteinemia
- Wilson disease
- Huntington disease
- Drug-induced movement disorder, eg, tardive dyskinesia
- Creutzfeldt-Jakob disease
- Frontotemporal dementia
- Corticobasal syndrome
- Progressive supranuclear palsy
- Parkinson disease
- Lewy body dementia
- Neurodegeneration with brain iron accumulation
- Paraneoplastic syndromes
- Primary psychiatric disease