-transparent.png){kind=logo}
Twelve affected members from 3 families with autosomal dominant exudative vitreouretinopathy were examined, and the following conclusions were drawn: (1) There is great variability in the phenotypic expression of the abnormal gene, such that many patients have very mild disease which can be detected with certainty only by fluorescein angiography. (2) Gene penetrance is close to 100%. (3) Progress of fundus changes and visual threat is rare after 20 years of age.
Related Publications
R R Ober, and
A C Bird, and
A M Hamilton, and
K Sehmi
October 1983,
Archives of ophthalmology (Chicago, Ill. : 1960),
R R Ober, and
A C Bird, and
A M Hamilton, and
K Sehmi
June 1984,
Archives of ophthalmology (Chicago, Ill. : 1960),
R R Ober, and
A C Bird, and
A M Hamilton, and
K Sehmi
March 2016,
American journal of human genetics,
R R Ober, and
A C Bird, and
A M Hamilton, and
K Sehmi
February 2010,
American journal of human genetics,
R R Ober, and
A C Bird, and
A M Hamilton, and
K Sehmi
February 1985,
Ophthalmic paediatrics and genetics,
R R Ober, and
A C Bird, and
A M Hamilton, and
K Sehmi
October 1982,
The British journal of ophthalmology,
R R Ober, and
A C Bird, and
A M Hamilton, and
K Sehmi
January 1995,
German journal of ophthalmology,
R R Ober, and
A C Bird, and
A M Hamilton, and
K Sehmi
October 2015,
European journal of ophthalmology,
R R Ober, and
A C Bird, and
A M Hamilton, and
K Sehmi
October 2000,
Clinical genetics,
R R Ober, and
A C Bird, and
A M Hamilton, and
K Sehmi
January 2013,
Retinal cases & brief reports,
