Gerstmann syndrome is a permanent disorder. It will last an individual's lifetime.
Gerstmann-Straussler-Scheinker disease is always fatal.
There is no cure for Gerstmann syndrome. Neither children nor adults with this disorder will recover completely from its effects.
Gerstmann syndrome is a cluster of neurological symptoms that includes difficulty writing (dysgraphia or agraphia), difficulty with arithmetic (dyscalculia or acalculia), an inability to distinguish left from right.
The parietal lobe is responsible for Gerstmann syndrome, which is a neurological disorder characterized by difficulties with writing, calculations, finger agnosia, and left-right disorientation. Damage to the dominant hemisphere of the parietal lobe, particularly the angular gyrus, is often associated with the manifestation of Gerstmann syndrome symptoms.
Two types of Gerstmann syndrome have been identified: an acquired form that occurs in adults who have suffered brain injury through stroke or trauma, and a developmental form that has been noted in children.
In adults, Gerstmann syndrome may be acquired when bleeding into the brain during a stroke or after a traumatic head injury occurs in an area of the left parietal lobe called the angular gyrus.
The prognosis for males diagnosed with Wiskott-Adrich syndrome is poor.
Prognosis of eisenmengers sydrome
The prognosis of individuals with Lambert-Eaton myasthenic syndrome varies widely. In fact, the most important element of prognosis involves the prognosis associated with any existing cancer.
The prognosis of individuals with Lambert-Eaton myasthenic syndrome varies widely. In fact, the most important element of prognosis involves the prognosis associated with any existing cancer.
Locked-in syndrome has a very poor prognosis, although some individuals have lived as long as 18 years with the condition
Prognosis for DWM varies anywhere from excellent to fatal