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Deficiency of ferroxidase

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Description

Aceruloplasminemia is characterized by iron accumulation in the brain and viscera. The clinical triad of retinal degeneration, diabetes mellitus (DM), and neurologic disease is seen in individuals ranging from age 30 years to older than 70 years. The neurologic findings of movement disorder (blepharospasm, grimacing, facial and neck dystonia, tremors, chorea) and ataxia (gait ataxia, dysarthria) correspond to regions of iron deposition in the brain. Individuals with aceruloplasminemia often present with anemia prior to onset of DM or obvious neurologic problems. Cognitive dysfunction including apathy and forgetfulness occurs in more than half of individuals with this condition.

GeneReviews

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

184

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Genes

External Links

  • OMIM

    604290

  • Orphanet

    48818

  • HPO

    9959

  • Medgen

    C0878682

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