Fraser syndrome
Recessive genetic disorder involving eye and genital abnormalities / From Wikipedia, the free encyclopedia
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For the anatomical abnormality observed in 1964, see Frasier syndrome.
Fraser syndrome (also known as Meyer-Schwickerath's syndrome, Fraser-François syndrome, or Ullrich-Feichtiger syndrome) is an autosomal recessive congenital disorder,[1][2] identified by several developmental anomalies. Fraser syndrome is named for the geneticist George R. Fraser, who first described the syndrome in 1962.
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Fraser syndrome | |
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Bilateral cryptophthalmos with microphthalmos in the left ocular globe and abnormal right ocular globe in a female infant with Fraser syndrome. | |
Specialty | Medical genetics |
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