Literature DB >> 14669035

[Schnyder's crystalline corneal dystrophy. Further narrowing of the linkage interval at chromosome 1p34.1-p36?].

P Riebeling1, S Polz, F Tost, J S Weiss, H Kuivaniemi, M Hoeltzenbein.   

Abstract

BACKGROUND: Schnyder's crystalline corneal dystrophy (SCCD) is a rare autosomal dominant disease and can occur in association with hyperlipoproteinemia. The disease has been mapped to chromosome 1p34.1-p36. CASE REPORT: We report on a 66-year-old woman and her son with Schnyder's crystalline corneal dystrophy. The mother had type IV hyperlipoproteinemia and hypercholesterolemia while her son had hypercholesterolemia with elevated LDL-cholesterol. Analysis of microsatellite markers within the candidate interval of 1p34.1-p36 showed that the affected son and his unaffected brother had inherited different alleles only for the proximal marker D1S228 from their affected mother.
CONCLUSIONS: The haplotype analysis suggests that either recombination has occurred, which would allow the candidate interval to be narrowed down, or alternatively, the SCCD in the reported family is not linked to chromosome 1, which would be a first indication of genetic heterogeneity in this disease. To reduce the risk of cardiovascular disease, hyperlipidemia should always be excluded in patients with Schnyder's crystalline corneal dystrophy.

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Year:  2003        PMID: 14669035     DOI: 10.1007/s00347-003-0883-2

Source DB:  PubMed          Journal:  Ophthalmologe        ISSN: 0941-293X            Impact factor:   1.059


  19 in total

1.  Phototherapeutic keratectomy for Schnyder's crystalline corneal dystrophy.

Authors:  L G Paparo; C J Rapuano; I M Raber; S Grewal; E J Cohen; P R Laibson
Journal:  Cornea       Date:  2000-05       Impact factor: 2.651

2.  Chromosomal mapping and expression of the human B120 gene.

Authors:  T Takeuchi; M Furihata; H H Heng; H Sonobe; Y Ohtsuki
Journal:  Gene       Date:  1998-06-15       Impact factor: 3.688

3.  Progressive Schnyder's corneal dystrophy.

Authors:  H J Ingraham; H D Perry; E D Donnenfeld; D D Donaldson
Journal:  Ophthalmology       Date:  1993-12       Impact factor: 12.079

4.  Schnyder corneal crystalline dystrophy: description of a new family with evidence of abnormal lipid storage in skin fibroblasts.

Authors:  C Battisti; M T Dotti; A Malandrini; F Pezzella; A M Bardelli; A Federico
Journal:  Am J Med Genet       Date:  1998-01-06

5.  In vivo confocal microscopy of a family with Schnyder crystalline corneal dystrophy.

Authors:  M H Vesaluoma; T U Linna; E M Sankila; J S Weiss; T M Tervo
Journal:  Ophthalmology       Date:  1999-05       Impact factor: 12.079

6.  Disappearance of crystals in Schnyder's crystalline corneal dystrophy after epithelial erosion.

Authors:  K C Chern; D M Meisler
Journal:  Am J Ophthalmol       Date:  1995-12       Impact factor: 5.258

7.  [Current status of linkage studies for gene localization in corneal dystrophies].

Authors:  W Lisch; E G Weidle; C T Emmig; J Kömpf; M P Baur
Journal:  Fortschr Ophthalmol       Date:  1991

8.  Schnyder's dystrophy. Progression and metabolism.

Authors:  W Lisch; E G Weidle; C Lisch; T Rice; E Beck; G Utermann
Journal:  Ophthalmic Paediatr Genet       Date:  1986-03

9.  Schnyder crystalline dystrophy sine crystals. Recommendation for a revision of nomenclature.

Authors:  J S Weiss
Journal:  Ophthalmology       Date:  1996-03       Impact factor: 12.079

10.  [Possibilities of therapeutic photokeratotomy with the excimer laser in treatment of Schnyder crystalline corneal dystrophy].

Authors:  U Meier; C Anastasi; F Failla; F Simona
Journal:  Klin Monbl Augenheilkd       Date:  1998-05       Impact factor: 0.700

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  4 in total

1.  [Classification of biomedical research reports as a reference for evidence-based medicine in ophthalmology. A survey considering as example the journal Der Ophthalmologe].

Authors:  H P N Scholl; M Fleckenstein; T U Krohne; F G Holz
Journal:  Ophthalmologe       Date:  2005-12       Impact factor: 1.059

2.  Visual morbidity in thirty-four families with Schnyder crystalline corneal dystrophy (an American Ophthalmological Society thesis).

Authors:  Jayne S Weiss
Journal:  Trans Am Ophthalmol Soc       Date:  2007

3.  Mutations in the UBIAD1 gene, encoding a potential prenyltransferase, are causal for Schnyder crystalline corneal dystrophy.

Authors:  Andrew Orr; Marie-Pierre Dubé; Julien Marcadier; Haiyan Jiang; Antonio Federico; Stanley George; Christopher Seamone; David Andrews; Paul Dubord; Simon Holland; Sylvie Provost; Vanessa Mongrain; Susan Evans; Brent Higgins; Sharen Bowman; Duane Guernsey; Mark Samuels
Journal:  PLoS One       Date:  2007-08-01       Impact factor: 3.240

4.  Functional study of SCCD pathogenic gene UBIAD1 (Review).

Authors:  Jumin Xie; Lingxing Li
Journal:  Mol Med Rep       Date:  2021-08-09       Impact factor: 2.952

  4 in total

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