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Title: 46,XX gonadal dysgenesis with epibulbar dermoid. Author: Quayle SA, Copeland KC. Journal: Am J Med Genet; 1991 Jul 01; 40(1):75-6. PubMed ID: 1909490. Abstract: Pure gonadal dysgenesis with 46,XX genotype is a rare abnormality with unknown etiology. Although sensorineural deafness has been described with 46,XX gonadal dysgenesis, the majority of reported cases of 46,XX gonadal dysgenesis have no associated physical abnormalities. We report a patient with 46,XX gonadal dysgenesis associated with epibulbar dermoids and preauricular skin tags, the classic ocular and skin manifestations of Goldenhar sequence (oculoauricular vertebral dysplasia). We propose that our patient may represent a new and previously unreported syndrome.[Abstract] [Full Text] [Related] [New Search]