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Syndrome reference sheet
Generated 13 Oct 2026
Neurology · Neurology / Neurocutaneous disorders

Neurofibromatosis type 2

Also known as: NF2-related schwannomatosis

Autosomal dominant tumor predisposition.

Medical specialty
Neurology
Subspecialty
Neurology / Neurocutaneous disorders
Sex & age distribution
Male: affected; Female: affected equally; Children: yes, severe form with early onset
Gene(s) involved
LZTR1, NF2, SMARCB1

Etiology & mechanism

NF2 loss.

Gene(s) involved (3)

LZTR1NF2SMARCB1

Symptoms & signs (5)

bilateral vestibular schwannomashearing lossimbalancemeningiomastinnitus
SyndromeScope — educational reference. Content is model-generated and not clinically verified; always confirm against OMIM, Orphanet and GeneReviews before clinical use.