Disease Directory Glaucoma secondary to spherophakia/ectopia lentis and megalocornea
Rare Disease

Glaucoma secondary to spherophakia/ectopia lentis and megalocornea

Type

Malformation syndrome

Gene

LTBP2

About Glaucoma secondary to spherophakia/ectopia lentis and megalocornea

Glaucoma secondary to spherophakia/ectopia lentis and megalocornea is a rare disease catalogued by Orphanet (ORPHA:238763). It is associated with the LTBP2 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 Glaucoma secondary to spherophakia/ectopia lentis and megalocornea trials.

Search ClinicalTrials.gov for "Glaucoma secondary to spherophakia/ectopia lentis and megalocornea" or filter by Orphanet code ORPHA:238763 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:238763)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

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Find recruiting Glaucoma secondary to spherophakia/ectopia lentis and megalocornea trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Glaucoma secondary to spherophakia/ectopia lentis and megalocornea. Updated daily.