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Parkinsonian-pyramidal syndrome

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Description

A rare genetic neurological disorder with characteristics of the association of both parkinsonian (such as bradykinesia, rigidity and/or rest tremor) and pyramidal (such as increased reflexes, extensor plantar reflexes, pyramidal weakness or spasticity) manifestations, which vary according to the underlying associated disease (for example neurodegenerative disease, inborn errors of metabolism).

SNOMEDCT_US

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

66

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Genes

External Links

  • OMIM

    260300

  • Orphanet

    171695

  • HPO
  • Medgen

    C1850100

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