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Neurofibromatosis is a genetic disorder that comprises benign tumours on the skin and nerves. This disease stems from mutations in specific genes integral to regulating cell growth and differentiation. Neurofibromatosis can manifest through various symptoms, including the appearance of multiple cafés au lait spots and tumours on the skin and along nerves.
In Indore, neurofibromatosis cases are occasionally seen. Apollo Hospitals are well-equipped with some of the best neurofibromatosis treatment doctors to help manage and control this condition effectively. When it comes to neurofibromatosis management, Apollo Hospitals offers a leading-edge approach. Their commitment to advanced technology is evident in their state-of-the-art facilities and laboratories.
Neurofibromatosis can be categorised into three main types:
Neurofibromatosis Type 1 (NF1): The most common type, making up a vast majority of cases. It's chiefly characterised by multiple 'café au lait' spots and benign tumours underneath the skin, additionally posing a higher risk of other health problems.
Neurofibromatosis Type 2 (NF2): A less common form. Patients with NF2 experience bilateral vestibular schwannomas (VS) and other benign tumours in their brain and spinal cord.
Schwannomatosis (SWN): This is the rarest type of neurofibromatosis. It's characterized by the growth of multiple schwannomas, which are benign tumours that form on nerve roots and spinal nerves.
The symptoms of neurofibromatosis can vary according to its type and severity:
Café au lait spots are flat, light brown birthmarks that can appear anywhere on the skin
Neurofibromas are benign tumours that grow under the skin. They can be small, round or larger and more complex
Bone deformities caused by tumour growth in the spine can lead to conditions like scoliosis
Eye problems like Lisch nodules, cataracts and vision loss can occur due to tumours in the eyes
Neurofibromatosis doctors at Apollo Hospitals in Indore employ a combination of clinical examination, imaging tests, and genetic testing to diagnose neurofibromatosis:
Physical examination: A healthcare professional will look for café au lait spots and other physical signs of the condition.
Imaging tests: X-rays, CT scans, and MRIs are used to identify tumours in the brain, spinal cord, or elsewhere in the body.
Genetic testing: This helps identify the specific genetic mutation causing the condition.
While there is no cure for neurofibromatosis yet, various treatments can help manage symptoms and prevent complications. At Apollo Hospitals in Indore, you can trust some of the best doctors for neurofibromatosis treatment who offer:
Medications: Medications like over-the-counter pain relievers, stronger prescription pain medication, or nerve pain medications can be used to manage this discomfort.
Surgery: This is employed to remove tumours and alleviate symptoms such as pain and numbness.
Chemotherapy: This is used to treat certain types of tumours, such as optic gliomas.
Monitoring: Regular checkups are crucial to monitor the progression of the condition and detect any new symptoms or complications.
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H1 | Abacavir: Uses, Dosage, Side Effects, and More |
H2 | What is Abacavir? |
H2 | Uses of Abacavir |
H2 | Dosage and Administration |
H3 | Important Considerations |
H2 | Side Effects |
H3 | Common Side Effects |
H3 | Serious Side Effects |
H2 | Interaction with Other Medicines |
H3 | Benefits of Abacavir |
H2 | Frequently Asked Questions |
H2 | Brand Names |
H2 | Conclusion |
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