Microangiopathy of brain, retina and cochlea.
- Specialty
- Neurology
- Subspecialty
- Neurology / Neuro-ophthalmology
- Sex & age distribution
- Male: affected; Female: affected, 3:1 female predominance; Children: rare, typically ages 20–40
- Gene(s) involved
- None recorded
- Alternative names & eponyms
- Retinocochleocerebral vasculopathy
Etiology & mechanism
Autoimmune endotheliopathy.
Gene(s) involved (0)
No gene recorded for this syndrome.
Symptoms & signs (4)
In plain terms, someone with Susac syndrome may experience the following — click any to explore related syndromes:
Same gene(s)
Other syndromes that involve one of this syndrome's genes.
Overlapping symptoms
Other syndromes that share symptoms with this one.
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Shares symptoms with
1 shared
Acute fatty liver of pregnancy syndrome
encephalopathy
1 shared
Alport syndrome with diffuse leiomyomatosis
hearing loss
1 shared
Alström syndrome
hearing loss
1 shared
Ask–Upmark kidney syndrome
headache
1 shared
Barré–Liéou syndrome
headache
1 shared
Branchio-oto-renal syndrome
hearing loss
1 shared
Cerebral hyperperfusion syndrome
headache
1 shared
Chanarin–Dorfman syndrome
hearing loss
1 shared
CHARGE syndrome
hearing loss
1 shared
Cockayne syndrome
hearing loss
Shares genes with
None.
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