Multiple painful schwannomas without vestibular tumors.
- Specialty
- Oncology
- Subspecialty
- Oncology / Hereditary cancer syndromes
- Sex & age distribution
- Male: affected; Female: affected; Children: rare, onset in adulthood
- Gene(s) involved
- LZTR1, SMARCB1
- Alternative names & eponyms
- Schwannomatosis
Etiology & mechanism
SMARCB1 or LZTR1 mutation.
Gene(s) involved (2)
Symptoms & signs (4)
In plain terms, someone with Schwannomatosis 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
Chiari malformation syndrome
numbness
1 shared
Chronic exertional compartment syndrome
numbness
1 shared
Dhat syndrome
weakness
1 shared
Ectopic Cushing syndrome
weakness
1 shared
Hypermobile Ehlers–Danlos syndrome
chronic pain
1 shared
NARP syndrome
weakness
1 shared
Painful arc syndrome
weakness
1 shared
Parsonage–Turner syndrome
weakness
1 shared
Snapping hip syndrome
weakness
1 shared
Spinal cord compression syndrome
weakness
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