Literature DB >> 1909490

46,XX gonadal dysgenesis with epibulbar dermoid.

S A Quayle1, K C Copeland.   

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.

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Year:  1991        PMID: 1909490     DOI: 10.1002/ajmg.1320400114

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  2 in total

1.  The genetics of XX gonadal dysgenesis.

Authors:  K Aittomäki
Journal:  Am J Hum Genet       Date:  1994-05       Impact factor: 11.025

Review 2.  Primary ovarian insufficiency: an update.

Authors:  Leticia Cox; James H Liu
Journal:  Int J Womens Health       Date:  2014-02-20
  2 in total

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