Disease Directory Sensorineural hearing loss-spastic quadriplegia-intellectual disability syndrome
Rare Disease

Sensorineural hearing loss-spastic quadriplegia-intellectual disability syndrome

Type

Malformation syndrome

Gene

AFG2B

About Sensorineural hearing loss-spastic quadriplegia-intellectual disability syndrome

Sensorineural hearing loss-spastic quadriplegia-intellectual disability syndrome is a rare disease catalogued by Orphanet (ORPHA:659975). It is associated with the AFG2B 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 Sensorineural hearing loss-spastic quadriplegia-intellectual disability syndrome trials.

Search ClinicalTrials.gov for "Sensorineural hearing loss-spastic quadriplegia-intellectual disability syndrome" or filter by Orphanet code ORPHA:659975 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:659975)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

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Find recruiting Sensorineural hearing loss-spastic quadriplegia-intellectual disability syndrome trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Sensorineural hearing loss-spastic quadriplegia-intellectual disability syndrome. Updated daily.