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Achondroplasia is a genetic disorder with an autosomal dominant pattern of inheritance whose primary feature is dwarfism. [3] It is the most common cause of dwarfism [4] and affects about 1 in 27,500 people. [3] In those with the condition, the arms and legs are short, while the torso is typically of normal length. [3]
Dwarfism is a condition of people and animals marked by unusually small size or short stature. [1] In humans, it is sometimes defined as an adult height of less than 147 centimetres (4 ft 10 in), regardless of sex; the average adult height among people with dwarfism is 120 centimetres (4 ft).
Dwarfing is a process in which a breed of animals or cultivar of plants is changed to become significantly smaller than standard members of their species. The effect can be induced through human intervention or non-human processes, and can include genetic, nutritional or hormonal means.
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A charity fundraiser who lives with a form of dwarfism is celebrating five years in a job with people he says have been "really supportive since day one".
Dogs have long been man's best friend, living as our domesticated companions for as long as 32,000 years. Today, they are one of the most popular pets in the US, found in over 54 million American ...
Example of a pedigree chart using Ahnentafel numbering. A pedigree chart is a diagram that shows the occurrence and appearance of phenotypes [jargon] of a particular gene or organism and its ancestors from one generation to the next, [1] [2] [3] [unreliable source?] most commonly humans, show dogs, and race horses.
There are several ways to determine if a child has chondrodystrophy, including parent testing and x-rays. If the fetus is suspected of having chondrodystrophy, the parents can be tested to find out if the fetus in fact does have the disease. It is not until the baby is born that a diagnosis can be declared. [3]