Literature DB >> 6502411

Role of the neural crest in anterior segment development and disease.

G R Beauchamp, P A Knepper.   

Abstract

Certain eye and associated systemic developmental anomalies are apparently related by virture of a common neural crest origin. The development of the anterior segment is extremely complex and is dependent upon the presence or absence of certain local factors (including extracellular matrices and glycoproteins), inductors, receptors, and specific time sequencing. Understanding anterior segment anomalies and their systemic associations requires an understanding of neural crest proliferation and migration patterns; and they may be unified under the designation of neurocristopathies. Goldenhar's syndrome, not previously considered a neurocristopathy, may be considered one on the basis of the relationship between clinical findings and neural crest embryology.

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Mesh:

Year:  1984        PMID: 6502411     DOI: 10.3928/0191-3913-19841101-03

Source DB:  PubMed          Journal:  J Pediatr Ophthalmol Strabismus        ISSN: 0191-3913            Impact factor:   1.402


  16 in total

1.  Histopathological examination of two cases of anterior staphyloma associated with Peters' anomaly and persistent hyperplastic primary vitreous.

Authors:  A Matsubara; H Ozeki; N Matsunaga; M Nozaki; M Ashikari; S Shirai; Y Ogura
Journal:  Br J Ophthalmol       Date:  2001-12       Impact factor: 4.638

2.  Posterior axial corneal malformation and uveoretinal angiodysgenesis--a neurocristopathy?

Authors:  C M Mooy; B J Clark; W R Lee
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1990       Impact factor: 3.117

3.  Peter's anomaly in an infant with a mild degree of Axenfeld's anomaly.

Authors:  A Saitoh; A Ohira; T Amemiya
Journal:  Br J Ophthalmol       Date:  1995-09       Impact factor: 4.638

4.  A girl with Peters plus syndrome associated with myelomeningocele and chronic renal failure.

Authors:  Osamu Motoyama; Hiroko Arai; Ryoko Harada; Kei Hasegawa; Kikuo Iitaka
Journal:  Clin Exp Nephrol       Date:  2010-04-28       Impact factor: 2.801

5.  Phenotype of autosomal recessive congenital microphthalmia mapping to chromosome 14q32.

Authors:  D A Bessant; K Anwar; S Khaliq; A Hameed; M Ismail; A M Payne; S Q Mehdi; S S Bhattacharya
Journal:  Br J Ophthalmol       Date:  1999-08       Impact factor: 4.638

6.  [Depression of respiration via toxic effects on the central nervous system following use of topical brimonidine in an infant with congenital glaucoma].

Authors:  K Heimann; T Peschgens; U Merz; H Hoernchen; T Wenzl
Journal:  Ophthalmologe       Date:  2007-06       Impact factor: 1.059

7.  Homozygous FOXE3 mutations cause non-syndromic, bilateral, total sclerocornea, aphakia, microphthalmia and optic disc coloboma.

Authors:  Manir Ali; Beatriz Buentello-Volante; Martin McKibbin; J Alberto Rocha-Medina; Narcis Fernandez-Fuentes; Wilson Koga-Nakamura; Aruna Ashiq; Kamron Khan; Adam P Booth; Grange Williams; Yasmin Raashid; Hussain Jafri; Aine Rice; Chris F Inglehearn; Juan Carlos Zenteno
Journal:  Mol Vis       Date:  2010-06-23       Impact factor: 2.367

8.  Willem Vrolik on cyclopia.

Authors:  B Baljet; F van der Werf; A J Otto
Journal:  Doc Ophthalmol       Date:  1991       Impact factor: 2.379

Review 9.  Corneal transparency: genesis, maintenance and dysfunction.

Authors:  Yureeda Qazi; Gilbert Wong; Bryan Monson; Jack Stringham; Balamurali K Ambati
Journal:  Brain Res Bull       Date:  2009-05-27       Impact factor: 4.077

10.  Clinical and genetic features of a dominantly-inherited microphthalmia pedigree from China.

Authors:  Changhong Yu; Zhengmao Hu; Jingzhi Li; Ting Liu; Kun Xia; Lixin Xie
Journal:  Mol Vis       Date:  2009-05-08       Impact factor: 2.367

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