Childhood glaucoma in neonatal Marfan syndrome resulting from a novel FBN1 deletion.

Subjects

Subjects :

Child, Preschool
DNA Mutational Analysis
Exons genetics
Female
Glaucoma diagnosis
Humans
Intraocular Pressure
Marfan Syndrome diagnosis
Tonometry, Ocular
Diseases in Twins genetics
Fibrillin-1 genetics
Glaucoma genetics
Marfan Syndrome genetics
Mutation
Sequence Deletion
Twins, Monozygotic genetics

Details

Language :

English

ISSN :

1715-3360

Volume :

52

Issue :

5

Database :

MEDLINE

Journal :

Canadian journal of ophthalmology. Journal canadien d'ophtalmologie

Publication Type :

Academic Journal

Accession number :

28985825

Full Text :

https://doi.org/10.1016/j.jcjo.2017.03.008