Ectopia lentis 2, isolated, autosomal recessive

An isolated ectopia lentis that has material basis in homozygous or compound heterozygous mutation in the ADAMTSL4 gene on chromosome 1q21.

Also known as: ECTOL2, ectopia lentis 2, isolated, autosomal recessive, ectopia lentis, isolated, autosomal recessive, autosomal recessive isolated ectopia lentis, autosomal recessive isolated ectopia lentis 2, ectopia lentis, isolated autosomal recessive

10 clinical trials for this condition and its sub-types.