Best Doctors for Neurofibromatosis in Mysore

Neurofibromatosis is a genetic condition that primarily affects the nervous system and skin. It is characterised by the growth of benign tumours, known as neurofibromas, which can result in a wide spectrum of symptoms, depending on the type and severity of the condition. The cause of neurofibromatosis traces back to mutations in certain genes responsible for cell growth and differentiation. Neurofibromatosis is rare.

Apollo Hospitals in Mysore has some of the best doctors for neurofibromatosis treatment who bring their vast experience and expertise to diagnose and manage this disease effectively. With some of the best neurofibromatosis doctors on board, patients can confidently entrust their well-being to Apollo Hospital, Mysore.

Search Result: 2

Dr Aumir Moin

MBBS, MD, DM (NEUROLOGY)

Registration No

60620

Language

English, हिंदी, ಕನ್ನಡ, اردو

16 years experience overall

Kuvempunagar , Mysore

MON- SAT | MON- SAT, MON- SAT | MON- SAT(04:00 PM-05:00 PM | 11:00 AM-12:45 PM | 04:00 PM-05:00 PM)

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Dr Somanath Vasudev

MD, DM (Neurology)

Registration No

67828

Language

English, ಕನ್ನಡ

16 years experience overall

Kuvempunagar , Mysore

MON- FRI | MON- SAT, MON- SAT | MON- FRI(04:00 PM-05:00 PM | 11:00 AM-12:45 PM | 04:00 PM-04:45 PM)

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Types/Stages of Neurofibromatosis

Neurofibromatosis can be classified into three main types:

Neurofibromatosis Type 1 (NF1): This is the most common form, characterised by multiple café au lait spots, benign tumours under the skin, and a higher susceptibility to other health issues including high blood pressure and skeletal abnormalities.
Neurofibromatosis Type 2 (NF2): A less common form, it involves bilateral vestibular schwannomas (VS) and other benign tumours in the brain and spinal cord.
Schwannomatosis (SWN): A rare form that features multiple schwannomas or benign tumours growing on nerve roots and spinal nerves.

Symptoms of Neurofibromatosis

The symptoms associated with neurofibromatosis can vary significantly, depending on the type and severity. Some common symptoms include:

Café au lait spots or flat, light brown birthmarks
Neurofibromas comprising benign tumours that grow under the skin or within the body
Bone deformities
Eye problems like Lisch nodules, cataracts or vision loss
Hearing loss is particularly prevalent in NF2 due to bilateral vestibular schwannomas.

Tests to Diagnose Neurofibromatosis

Diagnosing neurofibromatosis involves a combination of tests:

Physical Examination: The best doctors for neurofibromatosis treatment will look for physical signs like café au lait spots.
Imaging Tests: X-rays, CT scans and MRIs may be used to pinpoint tumours in the brain, spinal cord or elsewhere in the body.
Genetic Testing: Blood tests can help identify the specific gene mutation causing the condition.
Eye exams: These are used to check for Lisch nodules, cataracts, and vision loss.

Treatment or Surgery Options for Neurofibromatosis at Apollo Hospitals in Mysore

The best doctors for neurofibromatosis treatment, at Apollo Hospitals in Mysore, patients have access to various treatment options:

Surgery: Surgical procedures to remove tumours and alleviate symptoms such as pain and numbness.
Monitoring: Regular checkups are crucial to monitor the progression of the condition and detect any new symptoms or complications.
Assistive devices: If neurofibromatosis affects your hearing or vision, Corrective lenses for vision loss and hearing aids for hearing impairment.