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Cutis laxa, autosomal recessive, type 1B
rareAn 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.
- Identifiers
- MONDO:0013754 OMIM:614437
- Causal genes
- EFEMP2
- Also known as
- ARCL1B · cutis laxa, autosomal recessive, type IB
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