Literature DB >> 19539834

Juvenile neuronal ceroid lipofuscinosis (JNCL) and the eye.

Sara Bozorg1, Denia Ramirez-Montealegre, Mina Chung, David A Pearce.   

Abstract

Juvenile neuronal ceroid lipofuscinoses, or Batten disease, is the most common type of NCL in the United States and Europe. This devastating disorder presents with vision failure and progresses to include seizures, motor dysfunction, and dementia. Death usually occurs in the third decade, but some patients die before age twenty. Though the mechanism of visual failure remains poorly understood, recent advances in molecular genetics have improved diagnostic testing and suggested possible therapeutic strategies. The ophthalmologist plays a crucial role in both early diagnosis and documentation of progression of juvenile neuronal ceroid lipofuscinoses. We update Batten disease research, particularly as it relates to the eye, and present various theories on the pathophysiology of retinal degeneration.

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Year:  2009        PMID: 19539834      PMCID: PMC4139962          DOI: 10.1016/j.survophthal.2009.04.007

Source DB:  PubMed          Journal:  Surv Ophthalmol        ISSN: 0039-6257            Impact factor:   6.048


  98 in total

1.  Distinct patterns of serum immunoreactivity as evidence for multiple brain-directed autoantibodies in juvenile neuronal ceroid lipofuscinosis.

Authors:  M J Lim; J Beake; E Bible; T M Curran; D Ramirez-Montealegre; D A Pearce; J D Cooper
Journal:  Neuropathol Appl Neurobiol       Date:  2006-10       Impact factor: 8.090

2.  Batten disease: features to facilitate early diagnosis.

Authors:  J Collins; G E Holder; H Herbert; G G W Adams
Journal:  Br J Ophthalmol       Date:  2006-06-05       Impact factor: 4.638

Review 3.  Diagnosis of the neuronal ceroid lipofuscinoses: an update.

Authors:  Ruth E Williams; Laura Aberg; Taina Autti; Hans H Goebel; Alfried Kohlschütter; Tuula Lönnqvist
Journal:  Biochim Biophys Acta       Date:  2006-07-12

4.  Neuronal ceroid lipofuscinosis in Devon cattle is caused by a single base duplication (c.662dupG) in the bovine CLN5 gene.

Authors:  Peter J Houweling; Julie A L Cavanagh; David N Palmer; Tony Frugier; Nadia L Mitchell; Peter A Windsor; Herman W Raadsma; Imke Tammen
Journal:  Biochim Biophys Acta       Date:  2006-07-25

5.  Autophagy is disrupted in a knock-in mouse model of juvenile neuronal ceroid lipofuscinosis.

Authors:  Yi Cao; Janice A Espinola; Elisa Fossale; Ashish C Massey; Ana Maria Cuervo; Marcy E MacDonald; Susan L Cotman
Journal:  J Biol Chem       Date:  2006-05-19       Impact factor: 5.157

6.  Isolation of a novel gene underlying Batten disease, CLN3. The International Batten Disease Consortium.

Authors: 
Journal:  Cell       Date:  1995-09-22       Impact factor: 41.582

7.  Batten disease and the ATP synthase subunit c turnover pathway: raising antibodies to subunit c.

Authors:  D N Palmer; S L Bayliss; V J Westlake
Journal:  Am J Med Genet       Date:  1995-06-05

8.  Immunocytochemical studies in the ceroid-lipofuscinoses (Batten disease) using antibodies to subunit c of mitochondrial ATP synthase.

Authors:  V J Westlake; R D Jolly; S L Bayliss; D N Palmer
Journal:  Am J Med Genet       Date:  1995-06-05

9.  Prenatal diagnosis of Batten's disease.

Authors:  P B Munroe; J Rapola; H M Mitchison; A Mustonen; S E Mole; R M Gardiner; I Jarvela
Journal:  Lancet       Date:  1996-04-13       Impact factor: 79.321

10.  A frame shift mutation in canine TPP1 (the ortholog of human CLN2) in a juvenile Dachshund with neuronal ceroid lipofuscinosis.

Authors:  Tomoyuki Awano; Martin L Katz; Dennis P O'Brien; Istvan Sohar; Peter Lobel; Joan R Coates; Shahnawaz Khan; Gayle C Johnson; Urs Giger; Gary S Johnson
Journal:  Mol Genet Metab       Date:  2006-04-18       Impact factor: 4.204

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  15 in total

1.  [Juvenile neuronal ceroid lipofuscinosis. Ophthalmologic findings and differential diagnosis].

Authors:  T U Krohne; P Herrmann; J Kopitz; K Rüther; F G Holz
Journal:  Ophthalmologe       Date:  2010-07       Impact factor: 1.059

2.  Intraocular PAS-positive macrophages simulating Whipple's disease.

Authors:  Frederick A Jakobiec; Alison B Callahan; Fouad R Zakka
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2012-06-07       Impact factor: 3.117

3.  A novel deletion variant in CLN3 with highly variable expressivity is responsible for juvenile neuronal ceroid lipofuscinoses.

Authors:  Naser Gilani; Ehsan Razmara; Mehmet Ozaslan; Ihsan Kareem Abdulzahra; Saeid Arzhang; Ali Reza Tavasoli; Masoud Garshasbi
Journal:  Acta Neurol Belg       Date:  2021-03-30       Impact factor: 2.396

4.  Progressive retinal degeneration and accumulation of autofluorescent lipopigments in Progranulin deficient mice.

Authors:  Brian P Hafler; Zoe A Klein; Z Jimmy Zhou; Stephen M Strittmatter
Journal:  Brain Res       Date:  2014-09-16       Impact factor: 3.252

5.  [Neurological alterations and intellectual deficits with sudden visual loss in a 7-year-old boy].

Authors:  A Gotz-Wieckowska; M Pawlak; J Siwiec-Proscinska; M Seget
Journal:  Ophthalmologe       Date:  2013-05       Impact factor: 1.059

Review 6.  Vision loss in juvenile neuronal ceroid lipofuscinosis (CLN3 disease).

Authors:  Madhu M Ouseph; Mark E Kleinman; Qing Jun Wang
Journal:  Ann N Y Acad Sci       Date:  2016-01-08       Impact factor: 5.691

7.  Loss of CLN3, the gene mutated in juvenile neuronal ceroid lipofuscinosis, leads to metabolic impairment and autophagy induction in retinal pigment epithelium.

Authors:  Yu Zhong; Kabhilan Mohan; Jinpeng Liu; Ahmad Al-Attar; Penghui Lin; Robert M Flight; Qiushi Sun; Marc O Warmoes; Rahul R Deshpande; Huijuan Liu; Kyung Sik Jung; Mihail I Mitov; Nianwei Lin; D Allan Butterfield; Shuyan Lu; Jinze Liu; Hunter N B Moseley; Teresa W M Fan; Mark E Kleinman; Qing Jun Wang
Journal:  Biochim Biophys Acta Mol Basis Dis       Date:  2020-06-25       Impact factor: 6.633

8.  Spectrum of ocular manifestations in CLN2-associated batten (Jansky-Bielschowsky) disease correlate with advancing age and deteriorating neurological function.

Authors:  Anton Orlin; Dolan Sondhi; Matthew T Witmer; Matthew M Wessel; Jason G Mezey; Stephen M Kaminsky; Neil R Hackett; Kaleb Yohay; Barry Kosofsky; Mark M Souweidane; Michael G Kaplitt; Donald J D'Amico; Ronald G Crystal; Szilárd Kiss
Journal:  PLoS One       Date:  2013-08-28       Impact factor: 3.240

9.  Non-invasive assessment of retinal alterations in mouse models of infantile and juvenile neuronal ceroid lipofuscinosis by spectral domain optical coherence tomography.

Authors:  Janos Groh; David Stadler; Mathias Buttmann; Rudolf Martini
Journal:  Acta Neuropathol Commun       Date:  2014-05-10       Impact factor: 7.801

10.  OPTICAL COHERENCE TOMOGRAPHY IN JUVENILE NEURONAL CEROID LIPOFUSCINOSIS.

Authors:  Michael S Hansen; Marianne N Hove; Hanne Jensen; Michael Larsen
Journal:  Retin Cases Brief Rep       Date:  2016
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