Literature DB >> 1715674

Full-field electroretinograms in patients with the carbohydrate-deficient glycoprotein syndrome.

S Andréasson1, G Blennow, B Ehinger, K Strömland.   

Abstract

We examined five patients who had carbohydrate-deficient glycoprotein syndrome with full-field electroretinograms. Only two of the patients showed fundus changes typical for retinitis pigmentosa, whereas abnormal electroretinograms were seen in all patients. There was no recordable rod response; however, a delay in the cone b-wave implicit time was noted. All patients had nyctalopia. These observations suggest that patients with the carbohydrate-deficient glycoprotein syndrome have a progressive tapetoretinal degenerative disorder of the retinitis pigmentosa type with defined alterations in the electroretinogram.

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Year:  1991        PMID: 1715674     DOI: 10.1016/s0002-9394(14)76218-x

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


  10 in total

1.  Retinal characteristics of the congenital disorder of glycosylation PMM2-CDG.

Authors:  Dorothy A Thompson; Ruth J Lyons; Isabelle Russell-Eggitt; Alki Liasis; Herbert Jägle; Stephanie Grünewald
Journal:  J Inherit Metab Dis       Date:  2013-02-22       Impact factor: 4.982

2.  High residual activity of PMM2 in patients' fibroblasts: possible pitfall in the diagnosis of CDG-Ia (phosphomannomutase deficiency).

Authors:  S Grünewald; E Schollen; E Van Schaftingen; J Jaeken; G Matthijs
Journal:  Am J Hum Genet       Date:  2001-01-11       Impact factor: 11.025

Review 3.  The carbohydrate-deficient glycoprotein syndromes: an overview.

Authors:  J Jaeken; H Carchon
Journal:  J Inherit Metab Dis       Date:  1993       Impact factor: 4.982

4.  Carbohydrate deficient glycoprotein syndrome type I: ophthalmic aspects in four Sicilian patients.

Authors:  A Fiumara; R Barone; P Buttitta; M Di Pietro; A Scuderi; F Nigro; J Jaeken
Journal:  Br J Ophthalmol       Date:  1994-11       Impact factor: 4.638

5.  Evolution of ophthalmic and electrophysiological findings in identical twin sisters with the carbohydrate deficient glycoprotein syndrome type 1 over a period of 14 years.

Authors:  I Casteels; W Spileers; A Leys; L Lagae; J Jaeken
Journal:  Br J Ophthalmol       Date:  1996-10       Impact factor: 4.638

6.  Carbohydrate-deficient glycoprotein syndrome: clinical expression in adults with a new metabolic disease.

Authors:  H Stibler; G Blennow; B Kristiansson; H Lindehammer; B Hagberg
Journal:  J Neurol Neurosurg Psychiatry       Date:  1994-05       Impact factor: 10.154

7.  Ophthalmic findings in an infant with phosphomannomutase deficiency.

Authors:  Wyatt B Messenger; Paul Yang; Mark E Pennesi
Journal:  Doc Ophthalmol       Date:  2014-02-04       Impact factor: 2.379

8.  Ophthalmological and electrophysiological findings in monozygotic twin sisters with phosphomannomutase 2 deficiency (PMM2-CDG) over a period of 37 years.

Authors:  Ines Van Hees; Jaak Jaeken; Wouter Meersseman; Ingele Casteels
Journal:  GMS Ophthalmol Cases       Date:  2019-11-20

Review 9.  Congenital Disorders of Glycosylation from a Neurological Perspective.

Authors:  Justyna Paprocka; Aleksandra Jezela-Stanek; Anna Tylki-Szymańska; Stephanie Grunewald
Journal:  Brain Sci       Date:  2021-01-11

10.  Case Report: Multiple Retinal Astrocytic Hamartomas in Congenital Disorder of Glycosylation-Ia.

Authors:  Giulia Midena; Elisabetta Pilotto
Journal:  Front Med (Lausanne)       Date:  2022-02-14
  10 in total

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