Literature DB >> 18713575

The syndrome of optic nerve hypoplasia.

Mark Borchert1, Pamela Garcia-Filion.   

Abstract

The congenital malformation known as optic nerve hypoplasia (ONH) has been recognized in the past 30 years as an epidemic cause of congenital blindness. It was believed to occur either as an isolated anomaly or as a component of the syndrome of septo-optic dysplasia, which has evolved to include midline brain malformations and hypopituitarism. Evidence now suggests that ONH infrequently occurs in isolation. Most afflicted children will have hypothalamic dysfunction and/or neurodevelopmental impairment, regardless of MRI findings or severity of ONH. Adverse outcomes can often be ameliorated with early intervention. Thus, the syndrome of ONH should be suspected in all infants with signs of hypothalamic dysfunction or vision impairment.

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Year:  2008        PMID: 18713575     DOI: 10.1007/s11910-008-0061-7

Source DB:  PubMed          Journal:  Curr Neurol Neurosci Rep        ISSN: 1528-4042            Impact factor:   5.081


  87 in total

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Journal:  Arch Ophthalmol       Date:  1993-01

Review 10.  Septo-optic dysplasia - novel insights into the aetiology.

Authors:  Daniel Kelberman; Mehul Tulsidas Dattani
Journal:  Horm Res       Date:  2008-02-06
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  15 in total

1.  ATOH7 mutations cause autosomal recessive persistent hyperplasia of the primary vitreous.

Authors:  Lev Prasov; Tehmina Masud; Shagufta Khaliq; S Qasim Mehdi; Aiysha Abid; Edward R Oliver; Eduardo D Silva; Amy Lewanda; Michael C Brodsky; Mark Borchert; Daniel Kelberman; Jane C Sowden; Mehul T Dattani; Tom Glaser
Journal:  Hum Mol Genet       Date:  2012-05-29       Impact factor: 6.150

2.  Sequencing analysis of the ATOH7 gene in individuals with optic nerve hypoplasia.

Authors:  Sing-Hui Lim; Elizabeth St Germain; Khanh-Nhat Tran-Viet; Sandra Staffieri; Meghan Marino; Pr Hélène Dollfus; Erica B Nading; Sue Crowe; Glen Gole; Yaumara Perdomo-Trujillo; Michael Haybittel; James Elder; Valérie Pelletier; Elias Traboulsi; David Mackey; Terri L Young
Journal:  Ophthalmic Genet       Date:  2013-06-26       Impact factor: 1.803

3.  Magnetic resonance diffusion tensor imaging (MRDTI) and tractography in children with septo-optic dysplasia.

Authors:  Michael B Salmela; Keith A Cauley; Joshua P Nickerson; Chris J Koski; Christopher G Filippi
Journal:  Pediatr Radiol       Date:  2009-12-09

4.  Optic nerve hypoplasia in miniature poodle dogs: A preliminary genetic and candidate gene association study.

Authors:  Doreen Becker; Jessica K Niggel; Sue Pearce-Kelling; Ronald C Riis; Gustavo D Aguirre
Journal:  Vet Ophthalmol       Date:  2019-07-25       Impact factor: 1.644

5.  Light-adapted electroretinograms in optic nerve hypoplasia.

Authors:  Caroline Chaplin; Mark S Borchert; Cassandra Fink; Pamela Garcia-Filion; Daphne L McCulloch
Journal:  Doc Ophthalmol       Date:  2009-08-11       Impact factor: 2.379

Review 6.  Mitochondrial optic neuropathies - disease mechanisms and therapeutic strategies.

Authors:  Patrick Yu-Wai-Man; Philip G Griffiths; Patrick F Chinnery
Journal:  Prog Retin Eye Res       Date:  2010-11-26       Impact factor: 21.198

7.  Absence of age-related optic disk changes in young children with optic nerve hypoplasia.

Authors:  J Sutedja; P Garcia-Filion; C Fink; M Borchert
Journal:  Eye (Lond)       Date:  2014-02-21       Impact factor: 3.775

8.  Incidence and associated endocrine and neurologic abnormalities of optic nerve hypoplasia.

Authors:  Brian G Mohney; Ryan C Young; Nancy Diehl
Journal:  JAMA Ophthalmol       Date:  2013-07       Impact factor: 7.389

9.  Newborn thyroid-stimulating hormone in children with optic nerve hypoplasia: associations with hypothyroidism and vision.

Authors:  Cassandra Fink; Amy M Vedin; Pamela Garcia-Filion; Nina S Ma; Mitchell E Geffner; Mark Borchert
Journal:  J AAPOS       Date:  2012-10       Impact factor: 1.220

10.  Presenting features and long-term effects of growth hormone treatment of children with optic nerve hypoplasia/septo-optic dysplasia.

Authors:  Amy M Vedin; Hanna Karlsson; Cassandra Fink; Mark Borchert; Mitchell E Geffner
Journal:  Int J Pediatr Endocrinol       Date:  2011-11-15
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