autosomal recessive cutis laxa type IC
MeSH: C567716ORPHA: 221145
Overview
autosomal recessive cutis laxa type I that has material basis in homozygous or compound heterozygous mutation in the LTBP4 gene on chromosome 19q13
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
MeSH Code
C567716Orphanet Code
ORPHA:221145autosomal recessive cutis laxa type IC
| MeSH | C567716 |
| Orphanet | ORPHA:221145 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO