Don’t fight Blepharoptosis myopia ectopia lentis alone.Find your community on the free RareGuru App.
The following summary is from Orphanet, a European reference portal for information on rare diseases and orphan drugs.
Orpha Number: 1259
This syndrome is characterised by bilateral congenital blepharoptosis, ectopia lentis and high myopia.
It has been described in three members of one family (in a mother and her two daughters).
Transmission appears to be autosomal dominant.
Visit the Orphanet disease page for more resources.
Source: GARD Last updated on 05-01-20
Do you have information about a disease, disorder, or syndrome? Want to suggest a symptom?
Please send suggestions to RareGuru!