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A Rare Case of Unilateral Morning Glory Disc Anomaly in a Patient with Turner Syndrome: Report and Review of Posterior Segment Associations.
Sahni, Dev R; Wallace, Michael; Kanhere, Mansi; Al Saif, Hind; Couser, Natario.
Afiliação
  • Sahni DR; Virginia Commonwealth University School of Medicine, Richmond, VA, USA.
  • Wallace M; Department of Ophthalmology, Virginia Commonwealth University School of Medicine, Richmond, VA, USA.
  • Kanhere M; Department of Pediatrics, Division of Endocrinology, Virginia Commonwealth University School of Medicine, Richmond, VA, USA.
  • Al Saif H; Department of Pediatrics, Division of Clinical Genetics, Virginia Commonwealth University School of Medicine, Richmond, VA, USA.
  • Couser N; Department of Ophthalmology, Virginia Commonwealth University School of Medicine, Richmond, VA, USA.
Case Rep Ophthalmol Med ; 2018: 5969157, 2018.
Article em En | MEDLINE | ID: mdl-30050712
ABSTRACT
Turner syndrome is a common sex chromosome disorder affecting females. The disorder is caused by a partial loss, complete absence, or structural abnormality of one X chromosome. The clinical presentation is broad and ranges from the classic phenotype to minimal clinical manifestations. Ocular abnormalities associated with the syndrome are common. Reports describing abnormal eye features in individuals with Turner syndrome generally involve refractive errors (myopia or hyperopia), strabismus, and external or anterior segment abnormalities including hypertelorism, epicanthal folds, and ptosis. Posterior ocular segment anomalies involving the optic nerve and retina in Turner syndrome have been rarely reported. We report a rare presentation of an 11-year-old female with Turner syndrome and unilateral morning glory disc anomaly.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Revista: Case Rep Ophthalmol Med Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Revista: Case Rep Ophthalmol Med Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos