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Congenital rubella syndrome.

The British Journal of Ophthalmology, 01 Jan 1994, 78(1):79
https://doi.org/10.1136/bjo.78.1.79 PMID: 8110709 PMCID: PMC504701

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This is a comment on "Congenital rubella syndrome: ophthalmic manifestations and associated systemic disorders." Br J Ophthalmol. 1993 Jun;77(6):358-63.

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Br J Ophthalmol. 1994 Jan; 78(1): 79.
PMCID: PMC504701
PMID: 8110709

Congenital rubella syndrome.

A M Brooks and W E Gillies
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Selected References

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  • Givens KT, Lee DA, Jones T, Ilstrup DM. Congenital rubella syndrome: ophthalmic manifestations and associated systemic disorders. Br J Ophthalmol. 1993 Jun;77(6):358–363. [Europe PMC free article] [Abstract] [Google Scholar]
  • Gillies WE. Hypoplasia of the iris stroma in Gregg's syndrome unaccompanied by cataract but with deafness, rubella retinopathy and onset of glaucoma in adult or adolescent life. Aust J Ophthalmol. 1980 May;8(2):189–192. [Abstract] [Google Scholar]
  • Jerndal T. Dominant goniodysgenesis with late congenital glaucoma. A re-examination of Berg's pedigree. Am J Ophthalmol. 1972 Jul;74(1):28–33. [Abstract] [Google Scholar]
  • Martin JP, Zorab EC. Familial glaucoma. In nine generations of a South Hampshire family. Br J Ophthalmol. 1974 May;58(5):536–542. [Europe PMC free article] [Abstract] [Google Scholar]
  • Weatherill JR, Hart CT. Familial hypoplasia of the iris stroma associated with glaucoma. Br J Ophthalmol. 1969 Jul;53(7):433–438. [Europe PMC free article] [Abstract] [Google Scholar]
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