Literature DB >> 2063919

Congenital nystagmus in a (46,XX/45,X) mosaic woman from a family with X-linked congenital nystagmus.

D H Gutmann1, M L Brooks, B S Emanuel, D M McDonald-McGinn, E H Zackai.   

Abstract

X-linked congenital nystagmus is a rare disorder in which affected males manifest binocular uniplanar nystagmus with associated head oscillation. In the families previously reported, affected females have been described. We report on a multigeneration family with X-linked congenital nystagmus with an affected woman. She was a (46,XX/45,X) mosaic. Magnetic resonance images of the brain of affected individuals were normal.

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Year:  1991        PMID: 2063919     DOI: 10.1002/ajmg.1320390210

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


  3 in total

1.  Clinical features of affected males with X linked ocular albinism.

Authors:  S J Charles; J S Green; J W Grant; J R Yates; A T Moore
Journal:  Br J Ophthalmol       Date:  1993-04       Impact factor: 4.638

2.  Dual diagnoses in 152 patients with Turner syndrome: Knowledge of the second condition may lead to modification of treatment and/or surveillance.

Authors:  Kelly L Jones; Erin A McNamara; Mauro Longoni; Danny E Miller; Mersedeh Rohanizadegan; Laura A Newman; Frances Hayes; Lynne L Levitsky; Betty L Herrington; Angela E Lin
Journal:  Am J Med Genet A       Date:  2018-08-06       Impact factor: 2.802

3.  A novel mutation in FRMD7 causing X-linked idiopathic congenital nystagmus in a large family.

Authors:  Xiang He; Feng Gu; Yujing Wang; Jinting Yan; Meng Zhang; Shangzhi Huang; Xu Ma
Journal:  Mol Vis       Date:  2008-01-11       Impact factor: 2.367

  3 in total

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