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Choroid plexus papilloma

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Description

Choroid plexus tumors are of neuroectodermal origin and range from benign choroid plexus papillomas (CPPs) to malignant choroid carcinomas (CPCs). These rare tumors generally occur in childhood, but have also been reported in adults. Patients typically present with signs and symptoms of increased intracranial pressure including headache, hydrocephalus, papilledema, nausea, vomiting, cranial nerve deficits, gait impairment, and seizures (summary by Safaee et al., 2013).

OMIM

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

10

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Genes

External Links

  • OMIM

    260500

  • Orphanet

    2807

  • Medgen

    C0205770

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