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Neurofibromatosis

Neurofibromatosis type 1 (NF1) and type 2 (NF2) are genetically inherited diseases where the nerve tissue grows tumors.

Symptoms

• Café-au-lait spots (a type of birthmark)
• Freckles in the groin or underarm areas
• Benign tumors or lumps under the skin (neurofibromas)
• Tumor on the optic nerve (optic glioma)
• Lisch nodules (spots in the colored part of the eye)
• Bone defects such as bowing of the legs
• Inner ear tumors that can cause headaches, balance problems, or hearing loss

Risk Factors

• Family history
• Genetic Mutations

See our pre-conception and prenatal services

Genetic Test

• NF1
• NF2

Schedule an Appointment

To speak with a board-certified genetic counselor about your risks for this disease:

• Schedule genetic counseling appointment online
• Or call 1-800-975-4819
• Send email

Resources

Children’s Tumor Foundation

Neurofibromatosis, Inc.