Literature DB >> 6722075

A syndrome of congenital retinal dystrophy and saccade palsy--a subset of Leber's amaurosis.

A T Moore, D S Taylor.   

Abstract

Three children who presented in infancy with a severe visual defect and absent or barely recordable electroretinograms, with relatively well preserved visually evoked cortical potentials, were subsequently found to have vertical and horizontal saccade palsies with head thrusts but relatively good visual acuity. These children, who were clearly different from other infants with congenital retinal dystrophy, were also developmentally delayed and had systemic motor and speech defects, but their visual prognosis was relatively good. The recognition of their saccade palsy was delayed because their poor visual attention in infancy was ascribed purely to the tapetoretinal degeneration. We consider these patients represent a clear subset of those patients who are diagnosed as having congenital retinal dystrophy or Leber's amaurosis.

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Year:  1984        PMID: 6722075      PMCID: PMC1040367          DOI: 10.1136/bjo.68.6.421

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


  31 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.  Ophthalmoplegia and retinal degeneration associated with spinocerebellar ataxia.

Authors:  R S JAMPEL; H OKAZAKI; H BERNSTEIN
Journal:  Arch Ophthalmol       Date:  1961-08

3.  Amaurosis congenita (Leber).

Authors:  J SCHAPPERT-KIMMIJSER; H E HENKES; J VAN DEN BOSCH
Journal:  AMA Arch Ophthalmol       Date:  1959-02

4.  A type of congenital ocular motor apraxia presenting jerky head movements.

Authors:  D G COGAN
Journal:  Trans Am Acad Ophthalmol Otolaryngol       Date:  1952 Nov-Dec

5.  A disorder of rapid eye movements in Huntington's chorea.

Authors:  A Starr
Journal:  Brain       Date:  1967-09       Impact factor: 13.501

6.  Retinal aplasia in association with macular coloboma, keratoconus and cataract.

Authors:  D A Leighton; R Harris
Journal:  Clin Genet       Date:  1973       Impact factor: 4.438

7.  Congenital ocular motor apraxia: paediatric aspects.

Authors:  J Rendle-Short; B Appleton; J Pearn
Journal:  Aust Paediatr J       Date:  1973-10

8.  Ophthalmoplegia plus. The neurodegenerative disorders associated with progressive external ophthalmoplegia.

Authors:  D A Drachman
Journal:  Arch Neurol       Date:  1968-06

9.  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

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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  11 in total

1.  Abnormal vertical optokinetic nystagmus in infants and children.

Authors:  S Garbutt; C M Harris
Journal:  Br J Ophthalmol       Date:  2000-05       Impact factor: 4.638

2.  A case of cranial meningocele associated with Joubert syndrome.

Authors:  T Suzuki; M Hakozaki; N Kubo; K Kuroda; A Ogawa
Journal:  Childs Nerv Syst       Date:  1996-05       Impact factor: 1.475

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

Authors:  I M Russell-Eggitt; D S Taylor; P T Clayton; A Garner; A Kriss; J F Taylor
Journal:  Br J Ophthalmol       Date:  1989-04       Impact factor: 4.638

4.  Vermian agenesis without posterior fossa cyst.

Authors:  C Adamsbaum; V Moreau; C Bulteau; J Burstyn; F Lair Milan; G Kalifa
Journal:  Pediatr Radiol       Date:  1994

5.  Joubert syndrome: a clinico-radiological study.

Authors:  B Kendall; D Kingsley; S R Lambert; D Taylor; P Finn
Journal:  Neuroradiology       Date:  1990       Impact factor: 2.804

Review 6.  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

7.  Intermittent horizontal saccade failure ('ocular motor apraxia') in children.

Authors:  C M Harris; F Shawkat; I Russell-Eggitt; J Wilson; D Taylor
Journal:  Br J Ophthalmol       Date:  1996-02       Impact factor: 4.638

8.  Eye movement abnormalities in Joubert syndrome.

Authors:  Avery H Weiss; Dan Doherty; Melissa Parisi; Dennis Shaw; Ian Glass; James O Phillips
Journal:  Invest Ophthalmol Vis Sci       Date:  2009-05-14       Impact factor: 4.799

9.  Joubert Syndrome: Ophthalmological Findings in Correlation with Genotype and Hepatorenal Disease in 99 Patients Prospectively Evaluated at a Single Center.

Authors:  Brian P Brooks; Wadih M Zein; Amy H Thompson; Maryam Mokhtarzadeh; Daniel A Doherty; Melissa Parisi; Ian A Glass; May C Malicdan; Thierry Vilboux; Meghana Vemulapalli; James C Mullikin; William A Gahl; Meral Gunay-Aygun
Journal:  Ophthalmology       Date:  2018-07-25       Impact factor: 12.079

10.  Electroretinographic Assessment in Joubert Syndrome: A Suggested Objective Method to Evaluate the Effectiveness of Future Targeted Treatment.

Authors:  Giulio Ruberto; Vincenzo Parisi; Chiara Bertone; Sabrina Signorini; Mauro Antonini; Enza Maria Valente; Federica Manzoni; Valentina Serpieri; Riccardo Fausto; Luciano Quaranta
Journal:  Adv Ther       Date:  2020-07-15       Impact factor: 3.845

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