Gerstmann syndrome

MONDO:0005773

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.

Also known as: GS, Gerstmann Badal syndrome, Gerstmann tetrad, developmental Gerstmann syndrome

0 clinical trials for this condition and its sub-types, 0 tagged with Gerstmann syndrome itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Nervous system disorder (26588)

Including sub-types (0) Tagged with Gerstmann syndrome (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.