Disease Directory Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies
Connective Tissue

Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies

Type

Malformation syndrome

Gene

LTBP4

About Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies

Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies is a rare disease catalogued by Orphanet (ORPHA:221145). It is associated with the LTBP4 gene. Search below for active recruiting clinical trials from ClinicalTrials.gov, or visit the Orphanet expert page for specialist centres, natural history studies, and patient registries.

Clinical Trial Eligibility Tips

What to know before applying to Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies trials.

Search ClinicalTrials.gov for "Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies" or filter by Orphanet code ORPHA:221145 to find disease-specific studies.

Ask your specialist to refer you to a Centre of Expertise — Orphanet lists all accredited centres for this condition worldwide.

Natural history studies and patient registries often enrol before drug trials open — contact the Orphanet patient community first.

Patient Resources

Patient Organization

Orphanet

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Orphanet

European reference resource for rare diseases (ORPHA:221145)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

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Find recruiting Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies. Updated daily.