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Gerstmann syndrome

Disease definition

Gerstmann syndrome is a very rare neurological disorder characterized by the specific association of acalculia, finger agnosia, left-right disorientation, and agraphia, which is supposed to be secondary to a focal subcortical white matter damage in the parietal lobe.

ORPHA:221117

  • Synonym(s): -
  • Prevalence: -
  • Inheritance: -
  • Age of onset: -
  • ICD-10: F81.2
  • OMIM: -
  • UMLS: C0017494
  • MeSH: D005862
  • GARD: 8660
  • MedDRA: 10048608

Additional information

Further information on this disease

Specialised Social Services

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