Literature DB >> 511153

Primary mesodermal dysgenesis of the cornea (Peters' anomaly) in two brothers.

M Boel, J Timmermans, L Emmery, G Dralands, J P Fryns, H Van den Berghe.   

Abstract

In this report two brothers with a severe form of Peters' anomaly, i.e., primary dysgenesis mesodermalis of the cornea, are described. The third-degree consanguinity of the parents is an additional argument for the autosomal recessive inheritance of this condition.

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Year:  1979        PMID： 511153     DOI： 10.1007/bf00287184

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


  4 in total

1.  The occurrence of congenital keratoconus posticus circumscriptus in two siblings presenting a previously unrecognized syndrome.

Authors:  W P HANEY; H F FALLS
Journal:  Am J Ophthalmol       Date:  1961-07       Impact factor: 5.258

2.  A new oculocerebral syndrome with hypopigmentation.

Authors:  H E Cross; V A McKusick; W Breen
Journal:  J Pediatr       Date:  1967-03       Impact factor: 4.406

3.  Corneal clouding, subvalvular aortic stenosis, and midfacial hypoplasia associated with mental deficiency and growth retardation--a new syndrome?

Authors:  J P Fryns; H Van den Berghe
Journal:  Eur J Pediatr       Date:  1979-06-28       Impact factor: 3.183

4.  A syndrome characterized by corneal opacity, nystagmus, flexion contracture of the elbows, growth failure, and mental retardation.

Authors:  C Mietens; H Weber
Journal:  J Pediatr       Date:  1966-10       Impact factor: 4.406
  4 in total
  1 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
  1 in total

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