Neuhauser Eichner Opitz syndrome

Overview

Neuhauser-Eichner-Opitz syndrome is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Neuhauser-Eichner-Opitz syndrome, or a subtype of Neuhauser-Eichner-Opitz syndrome, affects less than 200,000 people in the US population. Source - National Institutes of Health (NIH)

Symptoms

The list of signs and symptoms mentioned in various sources for Neuhauser-Eichner-Opitz syndrome includes the 5 symptoms listed below: * Sudden truncal ataxia * Chorea * Athetosis * Absent deep tendon reflexes * Hyperextensible joints

Causes

etosis Chorea Hyperextensible joints

Prognosis

The 'prognosis' of Neuhauser-Eichner-Opitz syndrome usually refers to the likely outcome of Neuhauser-Eichner-Opitz syndrome. The prognosis of Neuhauser-Eichner-Opitz syndrome may include the duration of Neuhauser-Eichner-Opitz syndrome, chances of complications of Neuhauser-Eichner-Opitz syndrome, probable outcomes, prospects for recovery, recovery period for Neuhauser-Eichner-Opitz syndrome, survival rates, death rates, and other outcome possibilities in the overall prognosis of Neuhauser-Eichner-Opitz syndrome. Naturally, such forecast issues are by their nature unpredictable.