Systemic Features: No associated systemic disease has been described.
[disorders.eyes.arizona.edu]
Lattice dystrophy type II (Familial amyloidosis with lattice dystrophy, Meretoja syndrome) Mask-like facies Mask-like faciesl Blepharochalasis, Floppy ears Protruding lips
[slideshare.net]
Type II LCD (Meretoja) is due to mutations within the gelsolin gene on chromosome 9q34. 119, 120, 121, 122 LCD types IIIA, IV, VI, and VII are all related to point mutations
[entokey.com]