Edwards syndrome, also known as trisomy 18, is a genetic disorder caused by the presence of an extra copy of chromosome 18. Offspring with Edwards syndrome often exhibit severe developmental and physical disabilities, including growth retardation, congenital heart defects, and distinct facial features. The prognosis for infants with this condition is generally poor, with many not surviving beyond the first year of life. Those who do survive may face significant health challenges and require extensive medical care.
Edwards' syndrome cannot be prevented
Edwards' syndrome is caused by an extra copy of chromosome 18
John Edwards
Trisomy 18 syndrome
Edwards' syndrome
The cause of Edwards syndrome is and error in cell division, also known as meiotic disjunction. It can occur in 1 out of 2,500 pregnancies. Edwards syndrome goes by the term Trisomy 18 also.
Most children born with Edwards' syndrome appear weak and fragile, and they are often underweight
About 1 in 5,000 people eace year are diagnosed with Edwards Syndrome.
Syndactyly is a characteristic of Apert syndrome, Poland syndrome, Jarcho-Levin syndrome, oral-facial-digital syndrome, Pfeiffer syndrome, and Edwards syndrome
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Edwards syndrome, also known as trisomy 18, is a genetic disorder that is often severe and can be life-threatening. Many babies born with Edwards syndrome have significant health problems and developmental delays, which can result in a shortened lifespan. The majority of babies with Edwards syndrome do not survive beyond the first year of life.
No, CFC syndrome is caused by a sporadic mutation.