Disease Directory Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies
Rare Disease

Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies

Type

Disease

Gene

RHOA

About Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies

Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies is a rare disease catalogued by Orphanet (ORPHA:589608). It is associated with the RHOA 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 Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies trials.

Search ClinicalTrials.gov for "Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies" or filter by Orphanet code ORPHA:589608 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

Visit website ↗

Orphanet

European reference resource for rare diseases (ORPHA:589608)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

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Find recruiting Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies. Updated daily.