A autosomal recessive cutis laxa type I that has material basis in homozygous or compound heterozygous mutation in the LTBP4 gene on chromosome 19q13. The disease is MONDO_0013170 (cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies). Also known as: ARCL1C, Urban-Rifkin-Davis syndrome, autosomal recessive cutis laxa type 1C.