Disease Directory Keratosis follicularis spinulosa decalvans
Rare Disease

Keratosis follicularis spinulosa decalvans

Type

Disease

Gene

MBTPS2, SAT1, LRP1

About Keratosis follicularis spinulosa decalvans

Keratosis follicularis spinulosa decalvans is a rare disease catalogued by Orphanet (ORPHA:2340). It is associated with the MBTPS2, SAT1, LRP1 genes. 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 Keratosis follicularis spinulosa decalvans trials.

Search ClinicalTrials.gov for "Keratosis follicularis spinulosa decalvans" or filter by Orphanet code ORPHA:2340 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:2340)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

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Find recruiting Keratosis follicularis spinulosa decalvans trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Keratosis follicularis spinulosa decalvans. Updated daily.