Unfortunately, Patau Syndrome is not curable. Patau Syndrome is a rare genetic disorder caused by the presence of extra material from chromosome 13. It is a life-threatening disorder that usually results in severe birth defects, mental retardation, and, in most cases, early death.
Most infants born with Patau Syndrome have major physical and mental disabilities. Common physical problems include heart defects, cleft lip or palate, extra fingers and toes, and abnormal brain development. Mental retardation, seizures, and vision and hearing problems are also common. Babies born with Patau Syndrome usually do not survive past the age of one year.
Presently, there is no known cure for Patau Syndrome. Treatment usually focuses on managing symptoms and providing supportive care. This may involve physical therapy, occupational therapy, speech therapy, and other forms of supportive care. Medications may also be prescribed to control seizures and other symptoms.
Research is ongoing in the area of genetics and chromosomal abnormalities, which could potentially lead to new treatments and therapies for Patau Syndrome and other genetic disorders. However, at this time, there is no known cure.