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lymphedema & ptosis
Genetics:
- autosomal dominant
- associated with defects in FOXC2
Clinical manifestations:
- drooping of the upper eyelid (ptosis)
- - distichiasis (a double row of eyelashes)
- lymphedema affecting predominantly the lower limbs
- onset of lymphedema is around puberty
General
lymphedema
genetic disease of the lymphatic system
genetic syndrome (multisystem disorder)
Database Correlations
OMIM 153000
References
OMIM :accession 153000