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rare genetic disorder most often characterized by varying degrees of deafness, minor defects in structures arising from the neural. Waardenburg syndrome: Encyclopedia of Genetic Disorders. On the basis of the presence or absence of dystopia
canthorum (lateral displacement of the inner corner of the eye), Waardenburg syndrome type I (WS1) and. Format: File PDFAdobe Acrobat - View as HTML


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by sensorineural deafness in association with pigmentary