Clinical aspects: retinitis pigmentosa
Clinical aspects: retinitis pigmentosa
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临床方面:色素性视网膜炎
DOI:
10.1007/978-94-011-0533-0_18
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发表时间:
1995
影响因子:
2.7
通讯作者:
K. Rüther
中科院分区:
文献类型:
--
作者:
E. Zrenner;E. Apfelstedt‐Sylla;K. Rüther
The term ‘retinitis pigmentosa’ (RP) is used for a group of progressive retinal diseases representing one of the most frequent retinal hereditary dystrophies with a prevalence of 1:3000 to 1:5000. Detailed studies over the past years have shown that this condition is made up of genetically and clinically heterogeneous subtypes with different modes of genetic transmission and different types of progression (Merin and Auerbach, 1976; Heckenlively, 1988; Pagon, 1988). In their final stages, however, the disease conditions are identical showing diffusely affected photoreceptors and retinal pigment epithelial cells. Consequently, they are ophthalmologically difficult to distinguish from one another.
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影响因子:
4.2
作者:
JACOBSON, SG;KEMP, CM;NATHANS, J
通讯作者:
NATHANS, J
影响因子:
4.2
作者:
Thirkill,CE;Roth,AM;Takemoto,DJ;Tyler,NK;Keltner,JL
通讯作者:
Keltner,JL
DOI:
10.1073/pnas.88.20.9370
发表时间:
1991-10-01
影响因子:
11.1
作者:
DRYJA, TP;HAHN, LB;BERSON, EL
通讯作者:
BERSON, EL
DOI:
10.1073/pnas.90.9.3968
发表时间:
1993-05-01
影响因子:
11.1
作者:
SUBER, ML;PITTLER, SJ;HURWITZ, RL
通讯作者:
HURWITZ, RL