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Fig. 1 | Orphanet Journal of Rare Diseases

Fig. 1

From: Identification and in silico analysis of a spectrum of SLC4A11 variations in Indian familial and sporadic cases of congenital hereditary endothelial dystrophy

Fig. 1

Left to right: Slit lamp and AS-OCT images of the familial (F1 and F2) and sporadic (N1-N5) CHED cases. A cloudy and hazy cornea is observed using the slit lamp. The OCT images indicating edematous haze in the individuals. OD: Right eye; OS: Left Eye

Clinical slit lamp and anterior segment-optical coherence tomography (AS-OCT) images of the eyes of the recruited participants.

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Orphanet Journal of Rare Diseases

ISSN: 1750-1172