Human genetic facial disorders
This App Helps Diagnose Rare Genetic Disorders from a Picture
A Fierce Mother vs. a Fatal Mutation
17 Apr “Patients with rare diseases or genetic disorders go through a long period of Trained physicians can read a child's face like a map and detect any "This is a classic field for artificial intelligence because no human being.
A collection of disease information resources and questions answered by our Genetic and in Man (OMIM) is a catalog of human genes and genetic disorders .
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13 Jun A collection of disease information resources and questions answered by in Man (OMIM) is a catalog of human genes and genetic disorders.
Description:Signs and symptoms[ edit ] Individuals with Williams syndrome [1] The most common symptoms of Williams syndrome are heart defects and unusual facial features. Other symptoms include failure to gain weight appropriately in infancy failure to thrive and low muscle tone. Individuals with Williams syndrome tend to have widely spaced teeth, a long philtrum , and a flattened nasal bridge. Other symptoms may include gastrointestinal problems, such as severe or prolonged colic , [11] abdominal pain and diverticulitis , nocturnal enuresis bed wetting and urinary difficulties, dental irregularities and defective tooth enamel , as well as hormone problems, the most common being high blood calcium. This pattern is consistent with the visual-spatial disabilities and problems with behavioral timing often seen in Williams syndrome.
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