Literature DB >> 15300387

[Corneal anomalies in murine trisomy 16].

F Tost1, J Wolfinger, J Giebel, W Buselmaier.   

Abstract

BACKGROUND: The prevalence of human Down's syndrome is about 1:700. Investigations using animal models are therefore of clinical relevance for understanding its etiopathogenesis. No corneal changes have been reported with transgenic murine trisomy 16.
METHODS: A total of 20 fetal mice (n=40 eyes) with experimentally induced trisomy 16 were investigated from day 18 of pregnancy in order to determine whether visible developmental disorders of the cornea occur. All specimen were investigated microscopically in serial sections.
RESULTS: In addition to disturbances in systemic development, the transgenic mouse fetuses showed high rates of malformation of the eyes. Developmental and differentiation disorders of the corneal epithelial cell layers and structural disturbances of the corneal parenchyma were found. Our findings are the first demonstration of developmental disorders of the cornea in mouse fetuses with trisomy 16. These minor anomalies of the cornea could well have resulted in keratoconus if the animals had survived.
CONCLUSIONS: Our findings in transgenic mouse fetuses with trisomy 16 correspond to the clinical pattern of Down's syndrome in humans. Disturbed development of lids and lenses have a high prevalence, whereas corneal hypoplasia is found less often.

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Mesh:

Year:  2005        PMID: 15300387     DOI: 10.1007/s00347-004-1062-9

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


  25 in total

1.  Neurochemical characterization of embryonic brain development in trisomy 19 (Ts19) mice: implications of selective deficits observed for abnormal neural development in aneuploidy.

Authors:  M D Saltarelli; G L Forloni; M L Oster-Granite; J D Gearhart; J T Coyle
Journal:  Dev Genet       Date:  1987

2.  Capillary gas chromatography combined with ion trap detection for quantitative profiling of polyols in cerebrospinal fluid and plasma.

Authors:  H U Shetty; H W Holloway; S I Rapoport
Journal:  Anal Biochem       Date:  1995-01-01       Impact factor: 3.365

3.  Altered Ca2+ signaling and mitochondrial deficiencies in hippocampal neurons of trisomy 16 mice: a model of Down's syndrome.

Authors:  S Schuchmann; W Müller; U Heinemann
Journal:  J Neurosci       Date:  1998-09-15       Impact factor: 6.167

4.  Congenital colonic hypoganglionosis in murine trisomy 16--an animal model for Down's syndrome.

Authors:  A Leffler; T Wedel; L C Busch
Journal:  Eur J Pediatr Surg       Date:  1999-12       Impact factor: 2.191

5.  Examination of the eyelid closure defect in trisomy 16 mice.

Authors:  D A Lipski; E T Bersu
Journal:  Teratology       Date:  1990-09

6.  Impaired Ca-signaling in astrocytes from the Ts16 mouse model of Down syndrome.

Authors:  W Müller; U Heinemann; S Schuchmann
Journal:  Neurosci Lett       Date:  1997-02-21       Impact factor: 3.046

7.  Genesis and systematization of cardiovascular anomalies and analysis of skeletal malformations in murine trisomy 16 and 19. Two animal models for human trisomies.

Authors:  C Bacchus; H Sterz; W Buselmaier; S Sahai; H Winking
Journal:  Hum Genet       Date:  1987-09       Impact factor: 4.132

8.  Trisomy 16 in the mouse fetus associated with generalized edema and cardiovascular and urinary tract anomalies.

Authors:  S Miyabara; A Gropp; H Winking
Journal:  Teratology       Date:  1982-06

9.  Influence of mouse trisomy 16 on expression of specific genes.

Authors:  R Fundele; H Winking; E M Jägerbauer
Journal:  Dev Genet       Date:  1987

Review 10.  Genesis and systematization of cardiovascular anomalies in murine trisomy 16.

Authors:  W Buselmaier; C Bacchus; H Sterz
Journal:  Prog Clin Biol Res       Date:  1991
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