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Because polydactyly can be part of a syndrome (known genetic defect) or association (genetic defect not known), children with a congenital upper extremity deformity should be examined by a geneticist for other congenital anomalies. This should also be done if a syndrome is suspected, or if more than two or three generations of the family are ...
Polydactyly (from Greek πολυ-poly-'many') is when a limb has more than the usual number of digits. This can be: As a result of congenital abnormality in a normally pentadactyl animal. Polydactyly is very common among domestic cats. For more information, see polydactyly.
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.
All of the cats in the litter were born with polydactyly, a relatively common and harmless genetic variation in cats which means they are born with multiple extra toes. Related: 22-Pound ...
The polydactyly in these largely aquatic animals is not to be confused with polydactyly in the medical sense, i.e. it was not an anomaly in the sense it was not a congenital condition of having more than the typical number of digits for a given taxon. [1] Rather, it appears to be a result of the early evolution from a limb with a fin rather ...
Genomic imprinting, which determines whether some genes inherited from the mother and father get expressed. [10] The expressivity of a gene can be influenced by the environmental conditions. [11] For example, pigmentation in the fur of Himalayan rabbits is determined by the C gene, the activity of which is dependent on temperature. [12]
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.
Young–Madders syndrome, alternatively known as Pseudotrisomy 13 syndrome or holoprosencephaly–polydactyly syndrome, is a genetic disorder resulting from defective and duplicated chromosomes which result in holoprosencephaly, polydactyly, facial malformations and intellectual disability, with a significant variance in the severity of symptoms being seen across known cases. [1]