47 XYY and morning glory syndrome--a unique association.

Chew, Fiona L M; Visvaraja, Subrayan

Chew, Fiona L M; Visvaraja, Subrayan.

Affiliation

Chew FL; Department of Ophthalmology, University Malaya Medical Center, Malaysia. sabrefmin@yahoo.co.uk

J AAPOS ; 13(4): 406-7, 2009 Aug.

Article in En | MEDLINE | ID: mdl-19487143

Subject(s)

Encephalocele/genetics; Eye Abnormalities/genetics; Meningocele/genetics; Nose/abnormalities; Optic Disk/abnormalities; XYY Karyotype/genetics; Abnormalities, Multiple/genetics; Acrocallosal Syndrome/genetics; Child; Encephalocele/diagnosis; Eye Abnormalities/diagnosis; Frontal Lobe/abnormalities; Humans; Hypertelorism/diagnosis; Hypertelorism/genetics; Karyotyping; Magnetic Resonance Imaging; Male; Meningocele/diagnosis; Optic Disk/pathology; Syndrome

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Optic Disk / XYY Karyotype / Eye Abnormalities / Nose / Encephalocele / Meningocele Type of study: Diagnostic_studies / Risk_factors_studies Limits: Child / Humans / Male Language: En Journal: J AAPOS Journal subject: OFTALMOLOGIA / PEDIATRIA Year: 2009 Document type: Article Affiliation country: Malaysia Country of publication: United States

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