Literature DB >> 2713302

Leber's congenital amaurosis--a new syndrome with a cardiomyopathy.

I M Russell-Eggitt1, D S Taylor, P T Clayton, A Garner, A Kriss, J F Taylor.   

Abstract

Seven members of four families had nystagmus noted by 4 months of age, poor vision, photophobia, and a markedly reduced or absent electroretinogram. Six of these patients had a life threatening episode of cardiac failure in infancy. There were also two neonatal deaths, and one of the affected children died at 2 years and one at 19 years. The five surviving children are well, remain with nystagmus, and have visual acuities of less than 6/60, with the eldest two having lost perception of light. They have a short obese habitus distinct from that of their unaffected siblings and parents.

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Year:  1989        PMID: 2713302      PMCID: PMC1041708          DOI: 10.1136/bjo.73.4.250

Source DB:  PubMed          Journal:  Br J Ophthalmol        ISSN: 0007-1161            Impact factor:   4.638


  21 in total

1.  Disc oedema in congenital amaurosis of Leber.

Authors:  J T Flynn; R F Cullen
Journal:  Br J Ophthalmol       Date:  1975-09       Impact factor: 4.638

2.  Neurological abnormalities in congenital amaurosis of Leber. Review of 30 cases.

Authors:  M J Vaizey; M D Sanders; K C Wybar; J Wilson
Journal:  Arch Dis Child       Date:  1977-05       Impact factor: 3.791

3.  Ophthalmological findings in infantile type of so-called neuronal ceroid lipofuscinosis.

Authors:  C Raitta; P Santavuori
Journal:  Acta Ophthalmol (Copenh)       Date:  1973

4.  Mental retardation and neurologic involvement in patients with congenital retinal blindness.

Authors:  A S Dekaban
Journal:  Dev Med Child Neurol       Date:  1972-08       Impact factor: 5.449

5.  Congenital amaurosis of retinal origin (Leber).

Authors:  W C Edwards; R Macdonald; W D Price
Journal:  Am J Ophthalmol       Date:  1971-10       Impact factor: 5.258

6.  Photopic abnormalities in congenital stationary nightblindness.

Authors:  A E Krill; D Martin
Journal:  Invest Ophthalmol       Date:  1971-08

7.  Leber's congenital tapetoretinal degeneration.

Authors:  J Francois
Journal:  Int Ophthalmol Clin       Date:  1968

8.  Mitochondrial cytopathy. A multisystem disorder with ragged red fibres on muscle biopsy.

Authors:  J Egger; B D Lake; J Wilson
Journal:  Arch Dis Child       Date:  1981-10       Impact factor: 3.791

9.  Congenital amaurosis of retinal origin. Frequent association with neurological disorders.

Authors:  A Dekaban; R Carr
Journal:  Arch Neurol       Date:  1966-03

10.  Leber's congenital amaurosis. A retrospective study of 33 cases and a histopathological study of one case.

Authors:  K G Noble; R E Carr
Journal:  Arch Ophthalmol       Date:  1978-05
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  3 in total

1.  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

2.  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

Review 3.  Genetic Syndromes Associated with Congenital Cardiac Defects and Ophthalmologic Changes - Systematization for Diagnosis in the Clinical Practice.

Authors:  Priscila H A Oliveira; Beatriz S Souza; Eimi N Pacheco; Michele S Menegazzo; Ivan S Corrêa; Paulo R G Zen; Rafael F M Rosa; Claudia C Cesa; Lucia C Pellanda; Manuel A P Vilela
Journal:  Arq Bras Cardiol       Date:  2018-01       Impact factor: 2.000

  3 in total

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