Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies

A autosomal recessive cutis laxa type I that has material basis in homozygous or compound heterozygous mutation in the LTBP4 gene on chromosome 19q13

Also known as: ARCL1C, Urban-Rifkin-Davis syndrome, autosomal recessive cutis laxa type 1C, autosomal recessive cutis laxa type IC, cutis laxa with Severe pulmonary, gastrointestinal, and urinary abnormalities, cutis laxa, autosomal recessive, type 1C, cutis laxa, autosomal recessive, type IC

0 clinical trials for this condition and its sub-types, 0 tagged with Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies itself.