Blepharoptosis myopia ectopia lentis
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Description
The following summary is from Orphanet, a European reference portal for information on rare diseases and orphan drugs.
Orpha Number: 1259
Definition
This syndrome is characterised by bilateral congenital blepharoptosis, ectopia lentis and high myopia.
Epidemiology
It has been described in three members of one family (in a mother and her two daughters).
Genetic counseling
Transmission appears to be autosomal dominant.
Visit the Orphanet disease page for more resources.
Source: GARD Last updated on 05-01-20
Symptoms
Symptoms and their Known Frequencies
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