Polydactyly has been documented throughout history and is not attributed to a specific individual discovery. It occurs as a genetic variation where individuals are born with extra fingers or toes.
There is a 25% chance that the offspring will exhibit polydactyly if both parents are heterozygous for the trait.
Polydactyly can be corrected by surgical removal of the extra digit or partial digit
Polydactyly is the term for the presence of extra fingers. Syndactyly is the term for fused fingers.
Polydactyly can be diagnosed by external observation, x ray, and fetal sonogram
Polydactyly occurs during fetal development, typically when a baby is still in the womb. It is a congenital condition where a baby is born with extra fingers or toes. Polydactyly can be detected through prenatal ultrasound screening in some cases.
Polydactyly is typically autosomal, meaning it is not linked to the sex chromosomes. However, in some rare cases, polydactyly can be part of a sex-linked genetic disorder.
No. Polydactyly is purely an autosomal dominant genetic disorder and cannot be caused by any environmental stress.
polydactyly
There is no known prevention
Cases of polydactyly can be either genetic or occur sporadically. Genetic polydactyly is inherited and can be passed down in families, while sporadic polydactyly may result from random genetic mutations or other factors.
Polydactyly is a type of genetic mutation that results in individuals being born with extra fingers or toes. It is usually an inherited trait, although it can also occur spontaneously. Polydactyly is considered a rare condition.