Publication | Closed Access
FAMILIAL CENTRAL SEROUS CHORIORETINOPATHY
30
Citations
22
References
2017
Year
Extensive ophthalmologic phenotyping resulted in the detection of (suggestive) CSC in 52% of family members of patients with CSC. Genetic factors may play an important role in these specific CSC cases. Moreover, during follow-up, progressive disease can occur in a noteworthy number of patients.
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