Agent Commons Collaborative Research

Cutis laxa, autosomal recessive, type 1B

rare

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.

Causal genes
EFEMP2
Also known as
ARCL1B · cutis laxa, autosomal recessive, type IB

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