Adult Summary Report

Secondary Findings in Adult Subjects

Non-diagnostic, excludes newborn screening & prenatal testing/screening

• Status (Adult): Passed (Consensus scoring is Complete)
• Curation Status (Adult): Released 1.2.1
• Status (Pediatric): Incomplete (Consensus scoring is Incomplete)
• GENE/GENE PANEL: NF2
• Condition: Neurofibromatosis Type II
• Mode(s) of Inheritance: Autosomal Dominant

Actionability Assertion

• NF2 ⇔ 0007039 (neurofibromatosis, type ii; nf2): Assertion Pending

Final Consensus Scores

Gene Condition Pairs: NF2 ⇔ 0007039 (OMIM:101000)

Outcome / Intervention Pair	Severity	Likelihood	Effectiveness	Nature of the Intervention	Total Score
Vestibular schwannoma / MRI/Screening	2	3B	2B	3	10BB

1. What is the nature of the threat to health for an individual carrying a deleterious allele?

Prevalence of the Genetic Condition

In the past, the estimated prevalence of neurofibromatosis 2 (NF2) was estimated at 1:210,000. However, a recent 2010 study estimated a higher prevalence of 1:60,000. [1, 2, 3, 4]

Clinical Features

NF2 is characterized by the development of nervous system tumors (schwannomas and meningiomas), ocular abnormalities, and skin tumors. Bilateral vestibular schwannomas occur in 95% of adult patients; vestibular schwannoma growth rates are extremely variable, both between patients and over time in the same patient. Schwannomas typically affect both vestibular nerves, leading to hearing loss and deafness, tinnitus, dizziness and imbalance.
While the tumors caused by NF2 are not malignant, their anatomical location and multiplicity lead to great morbidity and early mortality. [3, 4, 1, 2]

Natural History

Average age of onset in individuals with NF2 is 18 to 24 years (range birth to 70 years). Nearly all affected individuals develop bilateral vestibular schwannomas by age 30. The average age of death is 36 years; actuarial survival from correct diagnosis is 15 years. NF2 has no racial or ethnic predilections.
Childhood-onset NF2 typically presents with non-8th nerve tumors and non-vestibular symptoms, while adult-onset NF2 typically presents with vestibular symptoms. Age at diagnosis, presence of intracranial meningiomas, type of treatment center and type of NF2 mutation are informative predictors of the risk of mortality. Age at diagnosis is, by far, the strongest single predictor. [3, 4, 1]

2. How effective are interventions for preventing harm?

Patient Management

At diagnosis, the following evaluations are recommended: head MRI, hearing evaluation including BAER, ophthalmologic evaluation, cutaneous evaluation, and a genetics consultation. (Tier 4) [1]

NF2 patients should be managed in specialty centers. NF2 patients who are managed at specialty centers have a significantly lower risk of mortality than those who are treated at non-specialty centers (relative risk 0.34, 95% CI 0.12-0.98). (Tier 2) [4]

Hearing preservation and augmentation are important in the management of individuals with NF2; all affected individual and their families should be referred to an audiologist. (Tier 2) [5]

A cervical spine scan should be performed before cranial surgery to prevent complications from manipulation under anesthesia. Lumbosacral imaging should be performed before regional analgesia is given. (Tier 3) [1]

Surveillance

MRI screening every 2 years for patients less than 20 and every 3 years for older patients should be sufficient for at-risk patients without tumors. The initial MRI scan could be at 10-12 years of age, or earlier in severely affected families. In 10% of cases, individuals with NF2 become symptomatic before 10 years of age. Once tumors are present, MRI screening should be at least annual until the individual growth rate is established. Annual audiological tests, including auditory brainstem response, may be useful. A full annual neurological examination is a wise precaution, with a spinal MRI every 2-3 years unless no tumors are present on the initial scan. (Tier 2) [4, 5]

Circumstances to Avoid

No circumstances-to-avoid recommendations have been provided for the Adult context.

3. What is the chance that this threat will materialize?

Mode of Inheritance

Autosomal Dominant

Prevalence of Genetic Variants

Prevalence of NF2 mutations was not identified.

Penetrance

Penetrance is close to 100%. Virtually all individuals who have a pathogenic germline mutation develop the disease in an average lifetime. (Tier 4) [1]

Relative Risk

Information on relative risk was not available for the Adult context.

Expressivity

Vestibular schwannoma growth rates are extremely variable, both between patients and over time in the same patient. Growth rates are highly variable even among multiple NF2 patients of similar ages in the same family. (Tier 3) [1, 3, 4]

4. What is the Nature of the Intervention?

Nature of Intervention

Management of NF2 requires a variety of non-invasive screening tests.

5. Would the underlying risk or condition escape detection prior to harm in the setting of recommended care?

Chance to Escape Clinical Detection

Regular screening (MRI, neurological, audiology) is recommended beginning at diagnosis, or earlier for family members. These screenings are above and beyond general population recommendations.

Date of Search: 06.20.2014

Reference List

1. Neurofibromatosis 2. Gene Reviews. (2011) Website: http://www.ncbi.nlm.nih.gov/books/NBK1201/

2. Neurofibromatosis type 2. Orphanet. (2009) Website: http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Expert=637

3. Baser ME, R Evans DG, Gutmann DH. Neurofibromatosis 2. Curr Opin Neurol. (2003) 16(1):27-33.

4. Evans DG, Baser ME, O'Reilly B, Rowe J, Gleeson M, Saeed S, King A, Huson SM, Kerr R, Thomas N, Irving R, MacFarlane R, Ferner R, McLeod R, Moffat D, Ramsden R. Management of the patient and family with neurofibromatosis 2: a consensus conference statement. Br J Neurosurg. (2005) 19(1):5-12.

5. Gutmann DH, Aylsworth A, Carey JC, Korf B, Marks J, Pyeritz RE, Rubenstein A, Viskochil D. The diagnostic evaluation and multidisciplinary management of neurofibromatosis 1 and neurofibromatosis 2. JAMA. (1997) 278(1):51-7.