Hereditary vitreoretinal degeneration and night blindness

V. Feiler-Ofry; A. Adam; L. Regenbogen; V. Godel; R. Stein

doi:10.1016/0002-9394(69)94263-9

Hereditary vitreoretinal degeneration and night blindness

V. Feiler-Ofry
, A. Adam
, L. Regenbogen
, V. Godel
, R. Stein

Research output: Contribution to journal › Article › peer-review

Abstract

A genetic disorder consisting of hyaloidoretinal degeneration associated with congenital night blindness, but without myopia, was found in two consecutive generations of a consanguineous Jewish-Iraqi family. Vitreous changes without the other anomalies were detected in four female relatives of the patients. The segregation of affected members in the family is consistent with several modes of inheritance. If the syndrome is X-linked, its locus is not close to the loci of Xg and of G6PD.

Original language	English
Pages (from-to)	553-558
Number of pages	6
Journal	American Journal of Ophthalmology
Volume	67
Issue number	4
DOIs	https://doi.org/10.1016/0002-9394(69)94263-9
State	Published - Apr 1969
Externally published	Yes

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title = "Hereditary vitreoretinal degeneration and night blindness",

abstract = "A genetic disorder consisting of hyaloidoretinal degeneration associated with congenital night blindness, but without myopia, was found in two consecutive generations of a consanguineous Jewish-Iraqi family. Vitreous changes without the other anomalies were detected in four female relatives of the patients. The segregation of affected members in the family is consistent with several modes of inheritance. If the syndrome is X-linked, its locus is not close to the loci of Xg and of G6PD.",

author = "V. Feiler-Ofry and A. Adam and L. Regenbogen and V. Godel and R. Stein",

year = "1969",

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AU - Feiler-Ofry, V.

AU - Adam, A.

AU - Regenbogen, L.

AU - Godel, V.

AU - Stein, R.

PY - 1969/4

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AB - A genetic disorder consisting of hyaloidoretinal degeneration associated with congenital night blindness, but without myopia, was found in two consecutive generations of a consanguineous Jewish-Iraqi family. Vitreous changes without the other anomalies were detected in four female relatives of the patients. The segregation of affected members in the family is consistent with several modes of inheritance. If the syndrome is X-linked, its locus is not close to the loci of Xg and of G6PD.

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Hereditary vitreoretinal degeneration and night blindness

Abstract

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