Literature DB >> 4061557

Peters' anomaly in association with ring 21 chromosomal abnormality.

G W Cibis, J Waeltermann, D J Harris.   

Abstract

A white boy, born at the gestational age of 39 weeks, had Peters' anomaly in association with a ring 21 chromosomal abnormality. Dysmorphic features included low-set ears, hypoplastic mandible, delicate, dry skin, narrow arched palate, wide spaced nipples and hypotonia. He also had a cloudy right cornea. Chromosomal analysis disclosed a ring 21 defect. The cornea had a paracentral white opacity with a loss of posterior stroma and no adherence of the iris to the leukoma. Intraocular pressure, the lens, and the posterior pole were normal.

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Year:  1985        PMID: 4061557     DOI: 10.1016/0002-9394(85)90632-4

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


  3 in total

1.  Heterogeneity in dominant anterior segment malformations.

Authors:  G E Holmström; W P Reardon; M Baraitser; J S Elston; D S Taylor
Journal:  Br J Ophthalmol       Date:  1991-10       Impact factor: 4.638

2.  Peters plus syndrome.

Authors:  Seema Kapoor; Sharmila Banerjee Mukherjee; Ritu Arora; Daraius Shroff
Journal:  Indian J Pediatr       Date:  2008-08-31       Impact factor: 1.967

Review 3.  Chromosome abnormalities and the genetics of congenital corneal opacification.

Authors:  A Mataftsi; L Islam; D Kelberman; J C Sowden; K K Nischal
Journal:  Mol Vis       Date:  2011-06-17       Impact factor: 2.367

  3 in total

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