A new pedigree with recessive CHED mapping to the CHED2 locus on 20p13

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Figure 1  .

Autosomal recessive CHED pedigree. Solid symbols show affected individuals and open symbols denote unaffected individuals, the spot indicates carrier status. Double marriage lines indicate a consanguineous pairing. The autosomal recessive and autosomal dominant CHED disease gene haplotypes are indicated, with allele fragment sizes shown for each genetic marker.

Figure 2  .

Opacified "ground glass" corneal appearance.