Gerstmann syndrome

From WikiMD's Wellness Encyclopedia

Gray726 inferior parietal lobule

Gerstmann syndrome is a rare neurological disorder characterized by a constellation of symptoms that typically include agraphia (inability to write), acalculia (inability to perform arithmetic calculations), finger agnosia (inability to distinguish the fingers on the hand), and left-right disorientation (inability to distinguish between the left and right sides of the body). This syndrome is named after the Austrian neurologist Josef Gerstmann, who first described the condition in the early 20th century.

Symptoms[edit | edit source]

The primary symptoms of Gerstmann syndrome include:

  • Agraphia: Difficulty in writing, which is not due to motor dysfunction but rather a cognitive impairment.
  • Acalculia: Difficulty in performing simple mathematical calculations.
  • Finger agnosia: Inability to recognize or differentiate between one's own fingers.
  • Left-right disorientation: Difficulty in distinguishing the left side of the body from the right side.

Causes[edit | edit source]

Gerstmann syndrome is most commonly associated with damage to the angular gyrus of the dominant hemisphere of the brain, which is typically the left hemisphere in right-handed individuals. This damage can result from various causes, including:

Diagnosis[edit | edit source]

Diagnosis of Gerstmann syndrome is primarily clinical and involves a thorough neurological examination. Neuroimaging techniques such as MRI and CT scan may be used to identify the underlying cause of the syndrome, such as a stroke or tumor.

Treatment[edit | edit source]

There is no specific treatment for Gerstmann syndrome. Management typically focuses on addressing the underlying cause and providing supportive therapies. These may include:

Prognosis[edit | edit source]

The prognosis for individuals with Gerstmann syndrome varies depending on the underlying cause and the extent of brain damage. Some individuals may experience significant improvement with appropriate therapy, while others may have persistent symptoms.

Related Pages[edit | edit source]

References[edit | edit source]

External Links[edit | edit source]


Contributors: Prab R. Tumpati, MD