Literature DB >> 2658617

Follow-up and diagnostic reappraisal of 75 patients with Leber's congenital amaurosis.

S R Lambert1, A Kriss, D Taylor, R Coffey, M Pembrey.   

Abstract

We reexamined 75 children in whom Leber's congenital amaurosis had been previously diagnosed. On review, 30 of these patients had an ocular or systemic disorder other than Leber's congenital amaurosis. The most common of these revised diagnoses were congenital stationary night blindness, achromatopsia, infantile-onset retinitis pigmentosa, Joubert's syndrome, Zellweger syndrome, and infantile Refsum's disease. Of the 45 patients with Leber's congenital amaurosis, mental retardation occurred in six patients, and visual deterioration in six patients. Leber's congenital amaurosis should only be diagnosed if other known ocular and systemic disorders have been carefully excluded.

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Year:  1989        PMID: 2658617     DOI: 10.1016/0002-9394(89)90259-6

Source DB:  PubMed          Journal:  Am J Ophthalmol        ISSN: 0002-9394            Impact factor:   5.258


  13 in total

1.  An unusual retinal vascular morphology in connection with a novel AIPL1 mutation in Leber's congenital amaurosis.

Authors:  S Heegaard; T Rosenberg; M Preising; J U Prause; T Bek
Journal:  Br J Ophthalmol       Date:  2003-08       Impact factor: 4.638

2.  Congenital retinal dystrophies: a study of early cognitive and visual development.

Authors:  M M Black; P M Sonksen
Journal:  Arch Dis Child       Date:  1992-03       Impact factor: 3.791

Review 3.  Gene therapy for Leber congenital amaurosis: advances and future directions.

Authors:  Robert B Hufnagel; Zubair M Ahmed; Zélia M Corrêa; Robert A Sisk
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2012-05-29       Impact factor: 3.117

4.  Light prevents exogenous 11-cis retinal from maintaining cone photoreceptors in chromophore-deficient mice.

Authors:  Jie Fan; Rosalie K Crouch; Masahiro Kono
Journal:  Invest Ophthalmol Vis Sci       Date:  2011-04-14       Impact factor: 4.799

5.  Visual acuity changes in patients with leber congenital amaurosis and mutations in CEP290.

Authors:  J Jason McAnany; Mohamed A Genead; Saloni Walia; Arlene V Drack; Edwin M Stone; Robert K Koenekoop; Elias I Traboulsi; Alison Smith; Richard G Weleber; Samuel G Jacobson; Gerald A Fishman
Journal:  JAMA Ophthalmol       Date:  2013-02       Impact factor: 7.389

Review 6.  The role of docosahexaenoic acid in retinal function.

Authors:  B G Jeffrey; H S Weisinger; M Neuringer; D C Mitchell
Journal:  Lipids       Date:  2001-09       Impact factor: 1.880

7.  Brain imaging studies in Leber's congenital amaurosis: new radiologic findings associated with the complex trait.

Authors:  Hee Kyung Yang; Jeong-Min Hwang; Sung Sup Park; Young Suk Yu
Journal:  Korean J Ophthalmol       Date:  2010-11-23

Review 8.  Joubert syndrome: insights into brain development, cilium biology, and complex disease.

Authors:  Dan Doherty
Journal:  Semin Pediatr Neurol       Date:  2009-09       Impact factor: 1.636

9.  Congenital fibrosis syndrome associated with central nervous system abnormalities.

Authors:  Christina Pieh; Hans Hilmar Goebel; Elizabeth C Engle; Irene Gottlob
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2003-06-18       Impact factor: 3.117

10.  Whole-exome sequencing identifies a novel ALMS1 mutation (p.Q2051X) in two Japanese brothers with Alström syndrome.

Authors:  Satoshi Katagiri; Kazutoshi Yoshitake; Masakazu Akahori; Takaaki Hayashi; Masaaki Furuno; Jo Nishino; Kazuho Ikeo; Hiroshi Tsuneoka; Takeshi Iwata
Journal:  Mol Vis       Date:  2013-11-24       Impact factor: 2.367

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