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Up to: Autosomal recessive cutis laxa type 1
Cutis laxa, autosomal recessive, type 1B
An autosomal recessive cutis laxa type I characterized by disturbed elastic fiber formation resulting in severe systemic connective tissue abnormalities that has material basis in homozygous or compound heterozygous mutation in the EFEMP2 gene on chromosome 11q13.
This condition has no sub-types.