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One of the polydactyl cats at the Ernest Hemingway House in Key West, Florida.This particular cat has seven (two extra) toes on each paw. A polydactyl cat is a cat with a congenital physical anomaly called polydactyly (also known as polydactylism or hyperdactyly), which causes the cat to be born with more than the usual number of toes on one or more of its paws.
Polydactyly also occurs in modern extant reptiles [82] and amphibians. [83] Polydactyly was a non-pathological, reacquired condition in extinct marine reptiles such as ichthyosaurs and hupehsuchians, some of which containing upwards of ten digits within their flippers. [84]
The hands and feet of people with ectrodactyly are often described as "claw-like" and may include only the thumb and one finger (usually either the little finger, ring finger, or a syndactyly of the two) with similar abnormalities of the feet. [7] People with oligodactyly often have full use of the remaining digits and adapt well to their ...
Inheritance of abnormal genes, e.g. polydactyly, ectrodactyly or brachydactyly, symptoms of deformed limbs then often occur in combination with other symptoms ; external causes during pregnancy (thus not inherited), e.g. via amniotic band syndrome; teratogenic drugs (e.g. thalidomide, which causes phocomelia) or environmental chemicals
This little Maine Coon kitten is one of a littler of nine Maine Coons born at a breeder in Salt Lake City, Utah. All of the cats in the litter were born with polydactyly, a relatively common and ...
Santos–Mateus–Leal syndrome, also known as Hirschsprung's disease-deafness-polydactyly syndrome is a very rare autosomal recessive limb malformation which is characterized by Hirschsprung's disease, feet and hand polydactyly, unilateral renal agenesis, and congenital hearing loss. [2] [3] Only 2 cases have been described in medical ...
Synpolydactyly is a combination of syndactyly and polydactyly. This image shows the hand morphology of an individual with polydactyly. SPD is inherited in an autosomal dominant pattern, meaning that an individual only needs to inherit one copy of the affected gene, also known as an allele, from either parent to potentially develop the condition.
The disease is not easily definable. The main form of diagnosis is presumptive, if the person has the usual triad of preaxial polydactyly with cutaneous syndactyly of at least one limb, macrocephaly, and hypertelorism. However, a definitive diagnosis can be made if there is a phenotype that is caused by a Gcps and a Gli3 gene mutation. It can ...